Azabicyclooctane derivatives useful in the treatment of cardiac arrhythmias

ABSTRACT

Compounds of formula I,                    
     wherein R 1 , R 2 , R 3  and R a  R h  are as defined in the specification. The compounds are useful in the prophylaxis and in the treatment of arrhythmias, in particular a trial and ventricular arrhythmias.

This application is a 371 of PCT/SE00/02064 filed Dec. 19, 2000, now WO 01/47893 Jul. 5, 2000.

FIELD OF THE INVENTION

This invention relates to novel pharmaceutically useful compounds, in particular compounds which are useful in the treatment of cardiac arrhythmias.

BACKGROUND AND PRIOR ART

Cardiac arrhythmias may be defined as abnormalities in the rate, regularity, or site of origin of the cardiac impulse or as disturbances in conduction which causes an abnormal sequence of activation. Arrhythmias may be classified clinically by means of the presumed site of origin (i.e. as supraventricular, including atrial and atrioventricular, arrhythmias and ventricular arrhythmias) and/or by means of rate (i.e. bradyarrhythmias (slow) and tachyarrhythmias (fast)).

In the treatment of cardiac arrhythmias, the negative outcome in clinical trials (see, for example, the outcome of the Cardiac Arrhythmia Suppression Trial (CAST) reported in New England Journal of Medicine, 321, 406 (1989)) with “traditional” antiarrhythmic drugs, which act primarily by slowing the conduction velocity (class I antiarrhythmic drugs), has prompted drug development towards compounds which selectively delay cardiac repolarization, thus prolonging the QT interval. Class III antiarrhythmic drugs may be defined as drugs which prolong the trans-membrane action potential duration (which can be caused by a block of outward K⁺ currents or from an increase of inward ion currents) and refractoriness, without affecting cardiac conduction.

One of the key disadvantages of hitherto known drugs which act by delaying repolarization (class m or otherwise) is that they all are known to exhibit a unique form of proarrhythmia known as torsades de pointes (turning of points), which may, on occasion be fatal. From the point of view of safety, the minimisation of this phenomenon (which has also been shown to be exhibited as a result of administration of noncardiac drugs such as phenotiazines, tricyclic antidepressants, antihistamines and antibiotics) is a key problem to be solved in the provision of effective antiarrhythmic drugs.

Antiarrhythmic drugs based on bispidines (3,7-diazabicyclo[3.3.1]nonanes), are known from inter alia international patent applications WO 91/07405 and WO 99/31100, European patent applications 306 871, 308 843 and 665 228 and U.S. Pat. Nos. 3,962,449, 4,556,662, 4,550,112, 4,459,301 and 5,468,858, as well as journal articles including inter alia J. Med. Chem. 39, 2559, (1996), Pharmacol. Res., 24, 149 (1991), Circulation, 90, 2032 (1994) and Anal. Sci. 9, 429, (1993). 3-Azabicyclo[3.2.1]octane compounds are neither disclosed nor suggested in any of these documents.

Compounds based on 3-azabicyclo[3.2.1]octanes are known for use in a variety of other medical applications including serotonin antagonism (as described in EP 212 802 and EP 645 391), neurokinin-I receptor antagonism (as described in WO 98/18788), nitric oxide synthase inhibition (as described in WO 97/36871) and analgesia (as described in Rico, B, et al., J. Heterocycl. Chem. 31(2), 313-318 (1994)). None of these documents either disclose or suggest the use of 3-azabicyclo[3.2.1]octane-based compounds as antiarrhythmic agents.

We have surprisingly found that a novel group of 3-azabicyclo[3.2.1]octane-based compounds exhibit electrophysiological activity, preferably class III electrophysiological activity, and are therefore expected to be useful in the treatment of cardiac arrhythmias.

DISCLOSURE OF THE INVENTION

According to the invention there is provided compounds of formula I,

wherein

the wavy bond represents optional endo- or exo-stereochemistry;

one of R¹ and R² represents R^(1a) and the other represents a fragment of the formula Ia,

R^(1a) represents C₁₋₁₂ alkyl (optionally substituted and/or terminated by one or more groups selected from halo, cyano, nitro, aryl, Het¹, —C(O)R^(7a), —OR^(7b), —N(R⁸)R^(7c), —C(O)XR⁹, —C(O)N(R¹⁰)R^(7d) and —S(O)₂R¹¹), Het², —C(O)R^(7a), —C(O)XR⁹, —C(O)N(R¹⁰)R^(7d) or —S(O)₂R¹¹;

R^(7a) to R^(7d) independently represent, at each occurrence when used herein, H, C₁₋₆ alkyl (optionally substituted and/or terminated by one or more substituents selected from —OH, C₁₋₆alkoxy, halo, cyano, nitro, aryl, Het³ and —NHC(O)R¹²), aryl or Het⁴, or R^(7d), together with R¹⁰, represents C₃₋₆ alkylene (which alkylene group is optionally interrupted by an O atom and/or is optionally substituted by one or more C₁₋₃ alkyl groups);

R¹² represents H, C₁₋₄ alkyl (optionally substituted and/or terminated by one or more substituents selected from halo, cyano, aryl and —NHC(O)R¹³) or aryl;

R¹³ represents H, C₁₋₄ alkyl or aryl;

R⁸ represents H, C₁₋₆ alkyl (optionally substituted and/or terminated by one or more substituents selected from —OH, halo, cyano, nitro and aryl), aryl, —C(O)R^(14a) or —C(O)OR^(14b);

R^(14a) and R^(14b) represent C₁₋₆ alkyl (optionally substituted and/or terminated by one or more substituents selected from —OH, halo, cyano, nitro and aryl) or aryl, or R^(14a) represents H;

X represents O or S;

R⁹ represents, at each occurrence when used herein, C₁₋₁₂ alkyl (optionally substituted and/or terminated by one or more substituents selected from —OH, halo, cyano, nitro, aryl, C₁₋₄ alkoxy, —SO₂R¹⁵ and Het⁵);

R¹⁵ represents C₁₋₆ alkyl or aryl;

R¹⁰ represents, at each occurrence when used herein, H, C₁₋₁₂ alkyl, C₁₋₆ alkoxy (which latter two groups are optionally substituted and/or terminated by one or more substituents selected from —OH, halo, cyano, nitro, C₁₋₄, alkyl and C₁₋₄ alkoxy), —D-aryl, —D-aryloxy, —D—Het⁶, —D—N(H)C(O)R^(16a), —D—S(O)₂R^(17a), —D—C(O)R^(16b), —D—C(O)OR^(17b), —D—C(O)N(R^(16c))R^(16d), or R¹⁰, together with R^(7d), represents C₃₋₄ alkylene (which alkylene group is optionally interrupted by an O atom and/or is optionally substituted.by one or more C₁₋₃ alkyl groups);

R^(16a) to R^(16d) independently represent H, C₁₋₆ alkyl (optionally substituted and/or terminated by one or more substituents selected from —OH, halo, cyano, nitro and aryl), aryl,) or R^(16c) and R^(16d) together represent C₃₋₆ alkylene;

R^(17a) and R^(17b) independently represent C₁₋₄ alkyl (optionally substituted and/or terminated by one or more substituents selected from —OH, halo, cyano, nitro and aryl) or aryl;

D represents a direct bond or C₁₋₆ alkylene;

R¹¹ represents, at each occurrence when used herein, C₁₋₆ alkyl (optionally substituted and/or terminated by one or more substituents selected from —OH, halo, cyano, nitro and aryl), aryl or Het⁷;

R⁴ represents H, halo, C₁₋₆ alkyl, —OR¹⁸, —E—N(R¹⁹)R²⁰ OR together with

R⁵, represents ═O;

R⁵ represents H, C₁₋₆ alkyl or, together with R⁴, represents ═O;

R¹⁸ represents H, C₁₋₆ alkyl, —E-aryl, —E—Het⁸, —C(O)R^(21a), —C(O)OR^(21b) or —C(O)N(R^(22a))R^(22b);

R¹⁹ represents H, C₁₋₆ alkyl, —E-aryl, —E—Het⁸, —C(O)R^(21a), —C(O)OR^(21b), —S(O))₂R^(21c), —[C(O)]_(p)N(R^(22a))R^(22b) or —C(NH)NH₂;

R²⁰ represents H, C₁₋₆ alkyl, —E-aryl or —C(O)R^(21d);

R^(21a) to R^(21d) independently represent, at each occurrence when used herein, C₁₋₆ alkyl (optionally substituted and/or terminated by one or more substituents selected from halo, aryl and Het⁹), aryl, Het¹⁰, or R^(21a) and R^(21d) independently represent H;

R^(22d) and R^(22b) independently represent, at each occurrence when used herein, H or C₁₋₆ alkyl (optionally substituted and/or terminated by one or more substituents selected from halo, aryl and Het¹¹), aryl, Het¹², or together represent C₃₋₆ alkylene, optionally interrupted by an O atom;

E represents, at each occurrence when used herein, a direct bond or C₁₋₄ alkylene;

p represents 1 or 2;

Het¹ to Het¹² independently represent, at each occurrence when used herein, five- to twelve-membered heterocyclic groups containing one or more heteroatoms selected from oxygen, nitrogen and/or sulfur, which groups are optionally substituted by one or more substituents selected from —OH, oxo, halo, cyano, nitro, C₁₋₆ alkyl, C₁₋₆ alkoxy aryl, aryloxy, —N(R^(23a))R^(23b), —C(O)R^(23c), —C(O)OR^(23d), —C(O)N(R^(23e))R^(23f), —N(R^(23g))C(O)R^(23h) and —N(R^(23i))S(O)₂R^(23j);

R^(23a) to R^(23j) independently represent C₁₋₆ alkyl, aryl or R^(23a) to R^(23i) independently represent H;

A represents a direct bond, —J—, —J—N(R²⁴)— or —J—O— (in which latter two groups, N(R²⁴)— or O— is attached to the carbon atom bearing R⁴ and R⁵);

B represents —Z—, —Z—N(R²⁵)—, —N(R²⁵)—Z—, —Z—S(O)₁₁—, —Z—O— (in which latter two groups, Z is attached to the carbon atom bearing R⁴ and R⁵), —N(R²⁵)C(O)O—Z—, (in which latter group, —N(R²⁵) is attached to the carbon atom bearing R⁹ and R¹⁰) or —C(O)N(R²⁵)— (in which latter group, —C(O) is attached to the carbon atom bearing R⁴ and R⁵);

J represents C₁₋₆ alkylene optionally substituted by one or more substituents selected from —OH, halo and amino;

Z represents a direct bond or C₁₋₄ alkylene;

R²⁴ and R²⁵ independently represent H or C₁₋₆ alkyl;

G represents CH or N;

R⁶ represents one or more optional substituents selected from —OH, cyano, halo, nitro, C₁₋₆ alkyl (optionally terminated by —N(H)C(O)OR^(26a)), C₁₋₆ alkoxy N—, —N(R^(27a))R^(27b), —C(O)R^(27c), —C(O)OR^(27d), —C(O)N(R)R^(27e))R^(27f), —N(R^(27g))C(O)R^(27h), —N(R^(27i))C(O)N(R^(27j))R^(27k), —N(R^(27m))S(O)₂R^(26b), —S(O)_(n)R^(26c), and/or —OS(O)₂R^(26d);

R^(26a) to R^(26d) independently represent C₁₋₆ alkyl;

R^(27a) to R^(27m) independently represent H or C₁₋₆ alkyl;

n represents, at each occurrence, 0, 1 or 2; and

R^(a) to R^(h) and R³ independently represent H or C₁₋₄ alkyl;

wherein each aryl and aryloxy group, unless otherwise specified, is optionally substituted;

or a pharmaceutically acceptable derivative thereof;

provided that

(a) when A represents —J—N(R²⁴)— or —J—O—, then:

(i) J does not represent C₁ alkylene; and

(ii) B does not represent —N(R²⁵)—, —N(R²⁵)—Z— (in which latter group N(R²⁵) is attached to the carbon atom bearing R⁴ and R⁵), —S(O)_(n)—, —O— or —N(R²⁵)C(O)O—Z— when R⁴ and R⁵ do not together represent ═O;

(b) when R⁴ represents —OR¹⁸ or —N(R¹⁹)(R²⁰), then:

(i) A does not represent —J—N(R²⁴)— or —J—O—; and

(ii) B does not represent —N(R²⁵)—, —N(R²⁵)—Z— (in which latter group N(R²⁵) is attached to the carbon atom bearing R⁴ and R⁵), —S(O)_(n)—, —O— or —N(R²⁵)C(O)O—Z—;

(c) when A represents a direct bond, then R⁴ and R⁵ do not together represent ═O; and

(d) the compound is not: (±) (8β)-4-amino-5-chloro-2-methoxy-N-(3-benzyl-3-azabicyclo-[3.2.1]oct-8-yl)benzamide; (S)-N-(3-benzyl-3-azabicyclo[3.2.1]oct-8-yl)-4-amino-5-chloro-2-(1-methyl-2-butynyl)oxybenzamide; or (S)-N-(3-benzyl-3-azabicyclo[3.2.1]oct-8-yl)-4-amino-5-chloro-2-(1-methyl-2-butynyl)oxybenzamide hydrochloride;

which compounds are referred to hereinafter as “the compounds of the invention”.

Unless otherwise specified, alkyl groups and alkoxy groups as defined herein may be straight-chain or, when there is a sufficient number (i.e. a minimum of three) of carbon atoms, be branched-chain and/or cyclic. Further, when there is a sufficient number (i.e. a minimum of four) of carbon atoms, such alkyl and alkoxy groups may also be part cyclic/acyclic. Such alkyl and alkoxy groups may also be saturated or, when there is a sufficient number (i.e. a minimum of two) of carbon atoms, be unsaturated and/or interrupted by one or more oxygen and/or sulfur atoms. Unless otherwise specified, alkyl and alkoxy groups may also be substituted by one or more halo, and especially fluoro, atoms.

Unless otherwise specified, alkylene groups as defined herein may be straight-chain or, when there is a sufficient number (i.e. a minimum of two) of carbon atoms, be branched-chain. Such alkylene chains may also be saturated or, when there is a sufficient number (i.e. a minimum of two) of carbon atoms, be unsaturated and/or interrupted by one or more oxygen and/or sulfur atoms. Unless otherwise specified, alkylene groups may also be substituted by one or more halo atoms.

The term “aryl”, when used herein, includes C₆₋₁₀ aryl groups such as phenyl, naphthyl and the like. The term “aryloxy”, when used herein includes C₆₋₁₀ aryloxy groups such as phenoxy, naphthoxy and the like. For the avoidance of doubt, aryloxy groups referred to herein are attached to the rest of the molecule via the O-atom of the oxy-group. Unless otherwise specified, aryl and aryloxy groups may be substituted by one or more substituents including —OH, halo, Het¹, cyano, nitro, C₁₋₆ alkyl, C₁₋₆ alkoxy, N(R^(27a))R^(27b), —C(O)R^(27c), —C(O)OR^(27d), —C(O)N(R^(27e))R^(27f), —N(R^(27g))C(O)R^(27h), —N(R^(27m))S(O)₂R^(26b), —S(O)_(n)R^(26c), and/or —OS(O)₂R^(26d) (wherein Het¹, R^(26b) to R^(26d), R^(27a) to R^(27m) and n are as hereinbefore defined). When substituted, aryl and aryloxy groups are preferably substituted by between one and three substituents. When aryl is substituted by one or more Het¹ group(s), any aryl group(s) that said Het¹ group(s) may be substituted with may not itself (themselves) be substituted by any Het¹ group(s).

The term “halo”, when used herein, includes fluoro, chloro, bromo and iodo. Het (Het¹, Het², Het³, Het⁴, Het⁵, Het⁶, Het⁷, Het⁸, Het⁹, Het¹⁰, Het¹¹ and Het¹²) groups that may be mentioned include those containing 1 to 4 heteroatoms (selected from the group oxygen, nitrogen and/or sulfur) and in which the total number of atoms in the ring system are between five and twelve. Het (Het¹, Het², Het³, Het⁴, Het⁵, Het⁶, Het⁷, Het⁸, Het⁹, Het¹⁰, Het¹¹ and Het¹²) groups may be fully saturated, wholly aromatic, partly aromatic and/or bicyclic in character. Heterocyclic groups that may be mentioned include benzodioxanyl, benzodioxepanyl, benzodioxolyl, benzofuranyl, benzofurazanyl, benzimidazolyl, benzomorpholinyl, benzothiophenyl, chromanyl, cinnolinyl, dioxanyl, furanyl, hydantoinyl, imidazolyl, imidazo[1,2-a]pyridinyl, indolyl, isoquinolinyl, isoxazolyl, maleimido, morpholinyl, oxazolyl, phthalazinyl, piperazinyl, piperidinyl, purinyl, pyranyl, pyrazinyl, pyrazolyl, pyridinyl, pyrimindinyl, pyrrolidinonyl, pyrrolidinyl, pyrrolinyl, pyrrolyl, quinazolinyl, quinolinyl, 3-sulfolenyl, tetrahydropyranyl, tetrahydrofuranyl, thiazolyl, thienyl, thiochromanyl, triazolyl and the like. Values of Het¹ that may be mentioned include maleimido and piperazinyl. Values of Het² that may be mentioned include thiazolyl. Values of Het that may be mentioned include hydantoinyl. Values of Het⁴ that may be mentioned include benzodioxanyl, benzofurazanyl, pyrazolyl and pyrrolyl. Values of Het⁵ that may be mentioned include morpholinyl, piperazinyl and pyridinyl. Values of Het⁶ that may be mentioned include isoxazolyl and tetrahydropyranyl. Values of Het⁷ that may be mentioned include imidazolyl, pyrazolyl, 3-sulfolenyl and thiazolyl. Substituents on Het (Het¹, Het², Het³, Het⁴, Het⁵, Het⁶, Het⁷, Het⁸, Het⁹, Het¹⁰, Het¹¹ and Het¹²) groups may, where appropriate, be located on any atom in the ring system including a heteroatom. The point of attachment of Het (Het¹, Het², Het³, Het⁴, Het⁵, Het⁶, Het⁷, Het⁸, Het⁹, Het¹⁰, Het¹¹ and Het¹²) groups may be via any atom in the ring system including (where appropriate) a heteroatom, or an atom on any fused carbocyclic ring that may be present as part of the ring system. Het (Het¹, Het², Het³, Het⁴, Het⁵, Het⁶, Het⁷, Het⁸, Het⁹, Het¹⁰, Het¹¹ and Het¹²) groups may also be in the N— or S-oxidised form.

Pharmaceutically acceptable derivatives include salts and solvates. Salts which may be mentioned include acid addition salts. Pharmaceutically acceptable derivatives also include, at the 3-azabicyclo[3.2.1]octane or (when G represents N) pyridyl nitrogens, C₁₋₄alkyl quaternary ammonium salts and N-oxides, provided that when a N-oxide is present:

(a) no Het (Het¹, Het², Het³, Het⁴, Het⁵, Het⁶, Het⁷, Het⁸, Het⁹, Het¹⁰, Het¹¹ and Het¹²) group contains an unoxidised S-atom; and/or

(b) n does not represent 0 when B represents —Z—S(O)_(n)—.

The compounds of the invention may exhibit tautomerism. All tautomeric forms and mixtures thereof are included within the scope of the invention.

The compounds of the invention may also contain one or more asymmetric carbon atoms and may therefore exhibit optical and/or diastereoisomerism. Diastereoisomers may be separated using conventional techniques, e.g. chromatography or fractional crystallisation. The various stereoisomers may be isolated by separation of a racemic or other mixture of the compounds using conventional, e.g. fractional crystallisation or HPLC, techniques. Alternatively the desired optical isomers may be made by reaction of the appropriate optically active starting materials under conditions which will not cause racemisation or epimerisation, or by derivatisation, for example with a homochiral acid followed by separation of the diastereomeric esters by conventional means (e.g. HPLC, chromatography over silica). All stereoisomers are included within the scope of the invention.

According to a further aspect of the invention, there is provided compounds of formula I as hereinbefore defined with the additional proviso that when Het¹ or Het⁴ represents piperazin-1-yl, then the piperazinyl group does not bear a 3,4-dichlorophenyl substituent.

According to a further aspect of the invention, there is provided compounds of formula I, as hereinbefore defined, but without proviso (d) and with the additional provisos that:

(i) when R¹ represents a fragment of formula Ia in which A represents J, B represents Z, and R⁴ and R⁵ represent H or C₁₋₆ alkyl; then R² does not represent C₁₋₁₀ alkyl substituted by Het¹ or —C(O)Het⁴ (wherein Het¹ or Het⁴ represents homopiperazin-1-yl, piperazin-1-yl or 1-imidazolidinyl, which homopiperazinyl, piperazinyl or imidazolidinyl group is substituted in the 4-, 4- or 3-position (respectively) by —C(O)R^(23c) (in which R^(23c) represents aryl) and (at one of the ring C-atoms) by aryl, and which homopiperazinyl, piperazinyl or imidazolidinyl group is further optionally substituted by C₁₋₆ alkyl), and which C₁₋₁₀ alkyl group is further optionally substituted by one substituent selected from optionally substituted phenyl, cyano, —OR^(7b), —N(R⁸)R^(7c), —C(O)OR⁹, —C(O)N(R¹⁰)R^(7d) (wherein R^(7b), R^(7c), R^(7d), R⁹ and R¹⁰ represent H, C₁₋₆ alkyl or optionally substituted phenyl), imidazolyl or optionally substituted indolyl;

(ii) when R^(a) to R^(h) and R³ all represent H; and R¹ represents a fragment of formula Ia in which the group —A—C(R⁴)(R⁵)—B— represents C₁₋₃ alkylene, G represents CH and R⁶ is absent; then R² does not represent —C(O)R^(7a), wherein R^(7a) represents phenyl substituted in the 2-position by C₃₋₆ alkynyloxy (optionally interrupted by oxygen), in the 4-position by —N(R^(27a))R^(27b) or —N(H)C(O)R^(27h) (wherein R^(27h) represents C₁₋₆ alkyl), and in the 5-position by halo; and

(iii) when R³ represents H; and R¹ represents a fragment of formula Ia in which the group —A—C(R⁴)(R⁵)—B— represents C₁₋₂ alkylene, G represents CH and R⁶ represents one or two substituents selected from C₁₋₆ alkyl (optionally interrupted by oxygen), C₁₋₄ alkoxy, CF₃, halo, nitro, —C(O)OH or —C(O)O—C₁₋₆ alkyl); then R² does not represent —C(O)R^(7a), wherein R^(7a) represents phenyl substituted in the 2-position by C₁₋₆ alkoxy, in the 4-position by —NH₂ or —N(H)C(O)R^(27h) (wherein R^(27h) represents C₁₋₆ alkyl), and in the 5-position by halo or —SR^(26c).

Abbreviations are listed at the end of this specification.

Preferred compounds of the invention include those in which:

R^(1a) represents C₁₋₈ alkyl (optionally substituted and/or terminated by one or more groups selected from halo, optionally substituted aryl, Het¹, —C(O)R^(7a), —OR^(7b), —N(R⁸)R^(7c), —C(O)XR⁹, —C(O)N(R¹⁰)R^(7d) and —S(O)₂R¹¹), Het², —C(O)R^(7a), —C(O)XR⁹, —C(O)N(R¹⁰)R^(7d) or —S(O)₂R¹¹;

R^(7a) to R^(7d) independently represent, at each occurrence, H, C₁₋₅ alkyl (optionally substituted and/or terminated by one or more substituents selected from —OH, C₁₋₄ alkoxy, halo, cyano, optionally substituted aryl, Het³ and —NHC(O)R¹²), optionally substituted aryl or Het⁴, or R^(7d), together with R¹⁰, represents C₃₋₆ alkylene;

R¹² represents C₁₋₃ alkyl (optionally substituted and/or terminated by one or more substituents selected from halo, aryl and —NHC(O)R¹³) or optionally substituted aryl;

R¹³ represents C₁₋₃ alkyl or aryl;

R⁸ represents H, C₁₋₄ alkyl (optionally substituted and/or terminated by optionally substituted aryl), optionally substituted aryl, —C(O)R^(14a), or —C(O) OR^(14b);

R^(14a) and R^(14b) represent C₁₋₄ alkyl (optionally substituted and/or terminated by aryl) or aryl;

R⁹ represents, at each occurrence, C₁₋₈ alkyl (optionally substituted and/or terminated by one or more substituents selected from —OH, halo, cyano, optionally substituted aryl, C₁₋₄ alkoxy, —SO₂R¹⁵ and Het⁵);

R¹⁵ represents C₁₋₄ alkyl or aryl;

R¹⁰ represents, at each occurrence, H, C₁₋₈ alkyl, C₁₋₄ alkoxy (which latter two groups are optionally substituted and/or terminated by one or more substituents selected from —OH, halo and C₁₋₄ alkoxy), —D-(optionally substituted aryl), —D-aryloxy, —D-Het⁶, —D—S(O)₂R^(17a), or R¹⁰, together with R^(7d), represents C₃₋₆ alkylene;

R^(17a) represents C₁₋₄ alkyl or optionally substituted aryl;

D represents a direct bond or C₁₋₃ alkylene;

R¹¹ represents, at each occurrence, C₁₋₅ alkyl (optionally substituted and/or terminated by one or more halo atoms), optionally substituted aryl or Het⁷;

R⁴ represents H, halo, C₁₋₂ alkyl, —OR¹⁸ or —E—N(R¹⁹)R²⁰;

R⁵ represents H, or C₁₋₂ alkyl;

R¹⁸ represents H, C₁₋₄ alkyl, —E-(optionally substituted aryl) or —E—Het⁸;

R¹⁹ represents H, C₁₋₄ alkyl, —E-aryl, —E—Het⁸, —C(O)R^(21a) or —C(O)OR^(21b);

R²⁰ represents H, C₁₋₄ alkyl or —E-aryl;

R^(21a) and R^(21b) independently represent C₁₋₄ alkyl (optionally substituted and/or terminated by one or more substituents selected from halo and aryl) or aryl;

E represents, at each occurrence, a direct bond or C₁₋₂ alkylene;

Het¹ to Het⁸ independently represent, at each occurrence, fully saturated, wholly aromatic, partly aromatic and/or bicyclic five- to twelve-membered heterocyclic groups containing between one and four heteroatoms selected from oxygen, nitrogen and/or sulfur, which groups are optionally substituted by one or more substituents selected from oxo, halo, cyano, C₁₋₅ alkyl, C₁₋₄ alkoxy, —N(R^(23a))R^(23b), —C(O)R^(23c), —C(O)OR^(23d), —C(O)N(R^(23e))R^(23f), and —N(R^(23g))C(O)R^(23h);

R^(23a) to R^(23h) independently represent H or C₁₋₃ alkyl;

A represents a direct bond or —J—;

B represents —Z—, —Z—N(R²⁵)—, —Z—S(O)_(n)— or —Z—O— (in which latter three groups, Z is attached to the carbon atom bearing R⁴ and R⁵);

J represents C₁₋₅ alkylene optionally substituted by one or more substituents selected from —OH, halo and amino;

Z represents a direct bond or C₁₋₃ alkylene;

n represents 0 or 2;

R²⁵ represents H or C₁₋₄ alkyl;

G represents CH;

R⁶ represents one or more optional substituents selected from —OH, cyano, halo, nitro, C₁₋₃ alkyl (optionally terminated by —N(H)C(O)OR^(26a)) and C₁₋₄ alkoxy;

R^(26a) represents C₁₋₄ alkyl;

R³ represents H or C₁₋₂ alkyl;

R^(a) to R^(h) all represent H.

More preferred compounds of the invention include those in which:

R^(1a) represents linear, branched or part cyclic/acyclic C₁₋₆ alkyl (which alkyl group is (i) optionally interrupted by one or more oxygen atoms; and/or (ii) optionally substituted and/or terminated by one or more groups selected from phenyl (optionally substituted by one or more substituents selected from halo and methoxy), Het¹ (optionally substituted by —C(O)R^(23c)), —C(O)R^(7a), —OR^(7b), —C(O)N(H)R¹⁰ and —S(O)₂R¹¹), Het², —C(O)R^(7a), —C(O)OR⁹, —C(O)N(H)R¹⁰ or —S(O)₂R¹¹;

R^(7a) and R^(7b) independently represent, at each occurrence, H, linear or branched C₁₋₅ alkyl (which alkyl group is (i) optionally unsaturated; and/or (ii) optionally substituted and/or terminated by one or more substituents selected from —OH, C₁₋₂ alkoxy, Het³ and —NHC(O)R¹²), phenyl (optionally substituted by halo or methoxy) or Het⁴ (optionally substituted by C₁₋₄ alkyl);

R¹² represents C₁₋₂ alkyl (optionally substituted and/or terminated by —NHC(O)R¹³);

R¹³ represents C₁₋₂alkyl;

R⁹ represents, at each occurrence, linear, branched or part cyclic/acyclic C₁₋₆ alkyl (which alkyl group is (i) optionally unsaturated; (ii) optionally interrupted by one or more oxygen atoms; and/or (iii) optionally substituted and/or terminated by one or more substituents selected from —OH, cyano, C₁₋₂ alkoxy, —SO₂R¹⁵ and Het⁵ (optionally substituted by —C(O)R^(23c)));

R¹⁵ represents C₁₋₂ alkyl;

R¹⁰ represents, at each occurrence, H, linear, branched or part cyclic/acyclic C₁₋₇ alkyl, (which alkyl group is (i) optionally interrupted by one or more oxygen atoms; and/or (ii) optionally substituted and/or terminated by C₁₋₂ alkoxy), phenyl (optionally substituted by one or more substituents selected from halo, methoxy, Het¹ and SR^(26c)), Het⁶ (optionally substituted by one or more C₁₋₂ alkyl groups) or —S(O)₂R^(17a);

R^(26c) represents C₁₋₂ alkyl optionally substituted by one or more halo atoms;

R^(17a) represents phenyl (optionally substituted by C₁₋₂ alkyl);

R¹¹ represents, at each occurrence, linear, branched or part cyclic/acyclic C₁₋₅ alkyl, phenyl (optionally substituted by one or more substituents selected from nitro, methoxy and N(H)C(O)R^(27h)) or Het⁷ (optionally substituted by one or more substituents selected from halo, C₁₋₂ alkyl and N(H)C(O)R^(23h));

R⁴ represents H, —OR¹⁸ or —N(H)R¹⁹;

R⁵ represents H;

R¹⁸ represents H or phenyl (optionally substituted by one or more substituents selected from OH and methoxy);

R¹⁹ represents H or —C(O)OR^(21b);

R^(21b) represents C₁₋₂ alkyl;

Het¹ to Het⁸ independently represent, at each occurrence, fully saturated, wholly aromatic, partly aromatic and/or bicyclic five- to twelve-membered heterocyclic groups containing between one and four heteroatoms selected from oxygen, nitrogen and/or sulfur;

R^(23c), R^(23h) and R^(27h) independently represent, at each occurrence, C₁₋₂ alkyl;

A represents a direct bond or —J—;

B represents —Z—, —Z—N(H)—, —Z—SO₂— or —Z—O— (in which latter three groups, Z is attached to the carbon atom bearing R⁴ and R⁵);

J represents C₁₋₃ alkylene optionally substituted by —OH or amino;

Z represents a direct bond or C₁₋₂ alkylene;

R⁶ represents one or two cyano groups;

R³ represents H or methyl.

Particularly preferred compounds of the invention include those in which:

R^(1a) represents —C(O)R^(7a), —C(O)N(H)R¹⁰ or —S(O)₂R¹¹;

R¹⁰ represents linear, branched or part cyclic/acyclic C₁₋₅ alkyl, (which alkyl group is optionally interrupted by one or more oxygen atoms);

R⁴ represents H, —OH or —NH₂;

A represents a direct bond or —J—;

B represents —Z—N(H)— or —Z—O— (in which latter two groups, Z is attached to the carbon atom bearing R⁴ and R⁵);

J represents C₁₋₃ alkylene;

R⁶ represents a cyano group in the position para to where B is attached;

R³ represents methyl.

Preferred compounds of the invention include the compounds of the Examples disclosed hereinafter.

Preparation

According to the invention there is also provided a process for the preparation of compounds of formula I which comprises:

(a) reaction of a compound of formula IIA or IIB,

wherein R¹, R², R³ and R^(a) to R^(h) are as hereinbefore defined, with a compound of formula III,

 R²⁸—L¹  III

wherein R²⁸ represents either R¹ or R² (as appropriate), L¹ represents a leaving group such as halo, alkanesulfonate, perfluoroalkanesulfonate, arenesulfonate, —OC(O)XR⁹, imidazole or R²⁹O— (wherein R²⁹ represents, for example, C₁₋₁₀ alkyl or azyl, which groups are optionally substituted by one or more halo or nitro groups) and R¹, R² and R⁹ are as hereinbefore defined, for example at between room and reflux temperature in the presence of a suitable base (e.g. triethylamine or potassium carbonate) and an appropriate organic solvent (e.g. dichloromethane, chloroform, acetonitrile, N,N-dimethylformamide, dimethylsulfoxide, THF, toluene or mixtures thereof);

(b) for compounds of formula I in which R¹ or R² (as appropriate) represents —C(O)XR⁹ or —C(O)N(R¹⁰)R^(7d), reaction of a compound of formula IVA or IVB,

wherein R³, R^(a) to R^(h) and L¹ are as hereinbefore defined and R¹ and R² represent a fragment of formula Ia, as hereinbefore defined, with a compound of formula V,

R³⁰—H  V

wherein R³⁰ represents —XR⁹ or —N(R¹⁰)R^(7d) and R^(7d), R⁹, R¹⁰ and X are as hereinbefore defined, for example under conditions described hereinbefore (process step (a));

(c) for compounds of formula I in which R¹ or R² (as appropriate) represents —C(O)N(H)R¹⁰, reaction of a compound of formula IIA or IIB (as appropriate), as hereinbefore defined (except that R¹ or R² (as appropriate) does not represent R^(1a)), with a compound of formula VI,

R¹⁰—N═C═O  VI

wherein R¹⁰ is as hereinbefore defined, for example at between 0° C. and reflux temperature in the presence of an appropriate organic solvent (e.g. dichloromethane), or via solid phase synthesis under conditions known to those skilled in the art;

(d) for compounds of formula I in which R¹ or R² (as appropriate) represents a fragment of formula Ia in which A represents CH₂ and R⁴ represents —OH or —N(H)R¹⁹, reaction of a compound of formula IIA or IIB, as hereinbefore defined (except that R¹ or R² (as appropriate) does not represent a fragment of formula Ia), with a compound of formula VII,

wherein Y represents O or N(R¹⁹) and R⁵, R⁶, R¹⁹, B and G are as hereinbefore defined, for example at elevated temperature (e.g. 60° C. to reflux) in the presence of a suitable solvent (e.g. a lower alkyl alcohol (e.g. IPA), acetonitrile, or a mixture of a lower alkyl alcohol and water);

(e) for compounds of formula I in which, in the fragment of formula Ia, B represents —Z—O—, reaction of a compound of formula VIIIA or VIIIB,

wherein R³, R⁴, R R^(a) to R^(h), A and Z are as hereinbefore defined, and R¹ and R² (as appropriate) are as hereinbefore defined (except that, in each case, they do not represent a fragment of formula Ia), with a compound of formula IX,

wherein R⁶ and G are as hereinbefore defined, for example under Mitsunobu-type conditions e.g. at between ambient (e.g. 25° C.) and reflux temperature in the presence of a tertiary phosphine (e.g. tributylphosphine or triphenylphosphine), an azodicarboxylate derivative (e.g. diethylazodicarboxylate or 1,1′-(azodicarbonyl)dipiperidine) and an appropriate organic solvent (e.g. dichloromethane or toluene);

(f) for compounds of formula I in which G represents N and B represents —Z—O—, reaction of a compound of formula VIIIA or VIIIB, as hereinbefore defined, with a compound of formula X,

wherein L² represents a leaving group such as halo, alkanesulfonate, perfluoroalkanesulfonate or arenesulfonate, and R⁶ is as hereinbefore defined, for example at between 10° C. and reflux temperature in the presence of a suitable base (e.g. sodium hydride) and an appropriate solvent (e.g. N,N-dimethylformamide);

(g) for compounds of formula I in which R⁴ represents —OR¹⁸, in which R¹⁸ represents C₁₋₆ alkyl, —E-aryl or —E—Het⁸, reaction of a corresponding compound of formula I in which R⁴ represents OH with a compound of formula X),

R^(18a)OH  XI

wherein R^(18a) represents C₁₋₆ alkyl, —E-aryl or —E—Het⁸, and E and Het⁸ are as hereinbefore defined, for example under Mitsunobu-type conditions (e.g. as described hereinbefore in process step (e));

(h) for compounds of formula I in which R⁴ represents —OR¹⁸, in which R¹⁸ represents C₁₋₆ alkyl, —E-aryl or —E—Het⁸, reaction of a compound of formula XIIA or XIIB,

wherein R¹ or R² (as appropriate) represents R^(7a), and R^(1a), R³, R⁵, R⁶, R^(a) to R^(h), A, B, G and L² are as hereinbefore defined, with a compound of formula XI, as hereinbefore defined, for example at between ambient (e.g. 25° C.) and reflux temperature, under Williamson-type conditions (i.e. in the presence of an appropriate base (e.g. KOH or NaH) and a suitable organic solvent (e.g. dimethylsulfoxide or N,Nimethylformamide)) (the skilled person will appreciate that certain compounds of formula XIIA and XIIB (e.g. those in which L² represents halo) may also be regarded as compounds of formula I as hereinbefore defined);

(i) for compounds of formula I in which R⁴ represents —E—NH₂, reduction of a compound of formula XIIIA or XIIIB,

wherein R¹ or R² (as appropriate) represents R^(1a), and R^(1a), R³, R⁵, R⁶, R^(a) to R^(h), A, B, E and G are as hereinbefore defined, for example by hydrogenation at a suitable pressure in the presence of a suitable catalyst (e.g. palladium on carbon) and an appropriate solvent (e.g. a water-ethanol mixture);

(j) for compounds of formula I in which R⁴ represents —E—N(R¹⁹)R²⁰, wherein R¹⁹ represents C₁₋₆ alkyl, —E-aryl —E—Het⁸, —C(O)R^(21a), C(O)OR^(21b), —S(O)₂R^(21c) or —C(O)N (R^(22a))R^(22b), reaction of a corresponding compound of formula I in which R⁴ represents —E—N(H)R²⁰ with a compound of formula XIV,

R^(19a)—L¹  XIV

wherein R^(19a) represents C₁₋₆ alkyl, —E-aryl —E—Het⁸, —C(O)R^(21a), —C(O)OR^(21b), —S(O)₂R^(21c) or —C(O)N(R^(22a))R^(22b) , and R^(21a), R^(21b), R^(21c) , R^(22a), R^(22b), Het⁸, E and L¹ are as hereinbefore defined, for example under conditions described hereinbefore (process step (a));

(k) for compounds of formula I in which R⁴ represents —E—N(R²⁰)C(O)N(H)R^(22a), reaction of a corresponding compound of formula I in which R⁴ represents —E—N(H)R²⁰ with a compound of formula XV,

R^(22a)—N═C═O  XV

wherein R^(22a) is as hereinbefore defined, for example under conditions described hereinbefore (process step (c));

(I) for compounds of formula I in which R⁴ represents —E—N(H)[C(O)]₂NH₂, reaction of a corresponding compound of formula I in which R⁴ represents —E—NH₂ with oxalic acid diamide, for example at between −10 and 25° C. in the presence of a suitable coupling agent (e.g. 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide), an appropriate activating agent (e.g. 1-hydroxybenzotriazole), a suitable base (e.g. triethylamine) and a reaction-inert solvent (e.g. N,N-dimethylformamide);

(m) for compounds of formula I in which R⁴ represents —E—N(H)C(NH)NH₂, reaction of a corresponding compound of formula I in which R⁴ represents —E—NH₂ with a compound of formula XVI,

R²⁹O—C(═NH)NH₂  XVI

or an N-protected derivative thereof, wherein R²⁹ is as hereinbefore defined, for example at between room and reflux temperature, optionally in the presence of a suitable solvent (e.g. toluene) and/or an appropriate acidic catalyst (e.g. acetic acid at, for example, 10 mol %);

(n) for compounds of formula I in which R⁴ represents —OR¹⁸, in which R¹⁸ represents —C(O)R^(21a), —C(O)OR^(21b) or —C(O)N(R^(22a))R^(22b), reaction of a corresponding compound of formula I in which R⁴ represents —OH with a compound of formula XVII,

R^(18b)—L³  XVII

wherein R^(18b) represents —C(O)R^(21a), —C(O)OR^(21b) or —C(O)N(R^(22a))R^(22b), L³ represents a leaving group such as halo, p-nitrophenoxy, —OC(O)R^(21a), —OC(O)OR^(21b), —OH or imidazole and R^(21a), R^(21b), R^(22a) and R^(22b) are as hereinbefore defined, for example at between −10° C. and reflux temperature in the presence of a suitable base (e.g. triethylamine, pyridine or potassium carbonate), an appropriate organic solvent (e.g. THF, dichloromethane or acetonitrile) and (where appropriate) a suitable coupling agent (e.g. 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide);

(o) for compounds of formula I in which R⁴ represents H or —OH and R⁵ represents H, reduction of a corresponding compound of formula I in which R⁴ and R⁵ together represent ═O, in the presence of a suitable reducing agent and under appropriate reaction conditions; for example, for formation of compounds of formula I in which R⁴ represents OH, reduction may be performed under mild reaction conditions in the presence of e.g. sodium borohydride and an appropriate organic solvent (e.g. THF); and for formation of compounds of formula I in which R⁴ represents H, reduction may be performed either under Wolff-Kischner conditions known to those skilled in the art or by activating the relevant C═O group using an appropriate agent (such as tosylhydrazine) in the presence of a suitable reducing agent (e.g. sodium borohydride or sodium cyanoborohydride) and an appropriate organic solvent (e.g. a lower (e.g. C₁₋₆) alkyl alcohol);

(p) for compounds of formula I in which R⁴ represents halo, substitution of a corresponding compound of formula I in which R⁴ represents —OH, using an appropriate halogenating agent (e.g. for compounds in which R⁴ represents fluoro, reaction with (diethylamino)sulfur trifluoride);

(q) for compounds of formula I in which R⁴ and R⁵ represent H, A represents —J—and B represents —N(R²⁵)Z— (wherein —N(R²⁵) is attached to the carbon atom bearing R⁴ and R⁵), reaction of a compound of formula XVIIIA or XVIIIB,

wherein R¹ or R² (as appropriate) represents R^(1a), and R^(1a), R³, R⁴, R⁵, R²⁵ R^(a) to R^(h) and J are as hereinbefore defined, with a compound of formula XIX,

wherein R⁶, G. Z and L² are as hereinbefore defined, for example at elevated temperature (e.g. 40° C. to reflux) in the presence of a suitable organic solvent (e.g. acetonitrile);

(r) for compounds of formula I in which A represents C₂ alkylene and R⁴ and R⁵ together represent ═O, reaction of a compound of formula IIA or IIB, as hereinbefore defined (except that R¹ or R² (as appropriate) does not represent a fragment of formula Ia), with a compound of formula XX,

wherein B, G and R⁶ are as hereinbefore defined, for example at between room and reflux temperature in the presence of a suitable base (e.g. triethylamine, potassium carbonate or tetrabutylammonium hydroxide) and an appropriate organic solvent (e.g. a lower alkyl (e.g. C₁₋₆) alcohol);

(s) for compounds of formula I in which R³ represents H and R² represents unsubstituted C₁₋₄ alkyl, reaction of a compound of formula XXI,

wherein R⁴, R⁵, R⁶, R^(a) to R^(h), A, B and G are as hereinbefore defined, with a compound of formula XXII,

R³¹—NH₂  XXII

wherein R³¹ represents unsubstituted C₁₋₄ alkyl, in the presence of a suitable reducing agent (e.g. sodium cyanoborohydride), for example at between room and reflux temperature, optionally in the presence of an appropriate solvent (e.g. a lower alkyl alcohol such as methanol) and/or a suitable catalyst (e.g. zinc chloride).

(t) for compounds of formula I in which R¹ represents —C(O)OR⁹ and R^(a) and/or R^(b) represent C₁₋₄ alkyl, reaction of a corresponding compound of formula I in which R¹ represents —C(O)OR⁹ and R^(a) and R^(b) represent H with one or more equivalents of a compound of formula XXIII,

R³²—L⁴  XXIII

wherein R³² represents C₁₋₄ alkyl and L⁴ is a leaving group such as halo, alkylsulfate, alkanesulfonate or arenesulfonate, in the presence of an appropriate strong base (e.g. butyllithium), for example at between −80° C. and room temperature in the presence of a suitable solvent (e.g. N,N,N′,N′-tetramethylethylene-diamine, THF or mixtures thereof).

(u) for compounds of formula I which are 3-azabicyclo[3.2.1]octane-nitrogen N-oxide derivatives, oxidation of the corresponding 3-azabicyclo[3.2.1]octane nitrogen of a corresponding compound of formula I, in the presence of a suitable oxidising agent (e.g. mCPBA), for example at 0° C. in the presence of a suitable organic solvent (e.g. dichloromethane);

(v) for compounds of formula I which are C₁₋₄ alkyl quaternary ammonium salt derivatives, in which the alkyl group is attached to a 3-azabicyclo[3.2.1]octane nitrogen, reaction, at the 3-azabicyclo[3.2.1]octane nitrogen, of a corresponding compound of formula I with a compound of formula XXIII, as hereinbefore defined, for example at room temperature in the presence of an appropriate organic solvent (e.g. N,N-dimethyl-formamide), followed by purification (using e.g. HPLC) in the presence of a suitable counter-ion provider (e.g. NH₄OAc); or

(w) conversion of one R⁶ substituent to another using techniques well known to those skilled in the art.

Compounds of formula IIA and IIB may be prepared by reaction of a compound of formula XXIV,

or an N-protected derivative thereof, wherein R³, R^(a) to R^(h) are as hereinbefore defined, with a compound of formula m as hereinbefore defined, for example as described hereinbefore for the synthesis of compounds of formula I (process step (a)), or, in the case of compounds of formula IIA or IIB wherein R¹ or R² (as appropriate) represents a fragment of formula Ia in which A represents CH₂ and R⁴ represents —OH or N(H)R¹⁹, wherein R¹⁹ is as hereinbefore defined, with a compound of formula VII as hereinbefore defined, for example as described hereinbefore for the synthesis of compounds of formula I (process step (d)).

Compounds of formula III may be prepared by standard techniques. For example, compounds of formula III in which R²⁸ represents a fragment of formula Ia, wherein:

(1) B represents —Z—O— may be prepared by coupling a compound of formula IX, as hereinbefore defined, to a compound of formula XXV,

 L²—Z—C(R⁴)(R⁵)—A—L²  XXV

wherein R⁴, R⁵, A, Z and L² are as hereinbefore defined, and the two L² groups may be the same or different; or

(2) B represents —C(O)N(R²⁵)— may be prepared by coupling a compound of formula XXVI,

wherein G, R⁶ and R²⁵ are as hereinbefore defined, to a compound of formula XXVII,

L⁵—C(O)—C(R⁴)(R)—A—L²  XXVI

wherein L⁵ represents a suitable leaving group (e.g. —OH or halo) and R⁴, R⁵, A and L² are as hereinbefore defined;

in both cases, under conditions which are well known to those skilled in the art.

Compounds of formula m in which R¹ represents a fragment of formula Ia, wherein A represents C₂ alkylene and R⁴ represents —OR¹⁸, in which R¹⁸ represents C₁₋₆ alkyl, —E-aryl or —E—Het⁸ may alternatively be prepared by reaction of a compound of formula XI, as hereinbefore defined, with a compound of formula XXVIII,

wherein R⁵, R⁶, R³², B and G are as hereinbefore defined, for example at between ambient temperature (e.g. 25° C.) and reflux temperature in the presence of a suitable base (e.g. potassium carbonate) and an appropriate organic solvent (e.g. acetonitrile), followed by conversion of the ester functionality to an L² group (in which L² is as hereinbefore defined), under conditions that are well known to those skilled in the art.

Compounds of formula IVA and IVB may be prepared by reaction of a compound of formula IIA or IIB, respectively, as hereinbefore defined, with a compound of formula XXIX,

L¹—C(O)—L¹  XXIX

wherein L¹ is as hereinbefore defined, and in which the two L¹ groups may be the same or different, for example at between 0° C. and reflux temperature in the presence of a suitable base (e.g. triethylamine or potassium carbonate) and an appropriate organic solvent (e.g. toluene or dichloromethane).

Compounds of formula VII may be prepared in accordance with techniques that are known to those skilled in the art. For example, compounds of formula VII in which:

(1) B represents —CH₂O— and Y represents O may be prepared by reaction of a compound of formula IX, as hereinbefore defined, with a compound of formula XXX

wherein R⁵ and L² are as hereinbefore defined, for example at elevated temperature (e.g. between 60° C. and reflux temperature) in the presence of a suitable base (e.g. potassium carbonate or NaOH) and an appropriate organic solvent (e.g. acetonitrile or toluene/water), or as otherwise described in the prior art;

(2) R⁵ represents H, B represents a direct bond, C₁₋₄ alkylene, —Z—N(R²⁵)—, —Z—S(O)_(n)— or —Z—O— (in which, in each case, the group Z represents C₁₋₄ alkylene attached to the carbon atom bearing R⁵) and Y represents O may be prepared by reduction of a compound of formula XXXIA or XXXIB,

wherein B^(a) represents —Z^(a)—N(R²⁵), —Z^(a)—S(O)_(n)— or —Z^(a)—O— (in which, in each case, the group Z^(a) represents a direct bond or C₁₋₃ alkylene attached to the carbon atom bearing R⁵), B^(b) represents a direct bond or C₁₋₄ alkylene, and R⁶, R²⁵, G and n are as hereinbefore defined, for example at between −15° C. and room temperature in the presence of a suitable reducing agent (e.g. NaBH₄) and an appropriate organic solvent (e.g. THF), followed by an internal displacement reaction in the resultant intermediate, for example at room temperature in the presence of a suitable base (e.g. potassium carbonate) and an appropriate organic solvent (e.g. acetonitrile);

(3) B represents a direct bond, C₁₋₄ alkylene, —Z—N(R²⁵)—, —Z—S(O)₂— or —Z—O— (in which, in each case, the group Z represents C₁₋₄ alkylene attached to the carbon atom bearing R⁵) and Y represents O may be prepared by oxidation of a compound of formula XXXIIA or XXXIIB,

wherein R⁵, R⁶, B^(a), B^(b) and G are as hereinbefore defined, in the presence of a suitable oxidising agent (e.g. mCPBA), for example by refluxing in the presence of a suitable organic solvent (e.g. dichloromethane); or

(4) B represents —Z—O—, in which group Z represents C₁₋₄ alkylene attached to the carbon atom bearing R⁵, and Y represents —N(R¹⁹), wherein R¹⁹ represents C(O)OR^(21b) or —S(O)₂R^(21c), may be prepared by cyclisation of a compound of formula XXXIII,

wherein R^(19b) represents —C(O)OR^(21b) or —S(O)₂R^(21c), Z^(b) represents C₁₋₄ alkylene and R⁵, R⁶, R^(21b), R^(21c), G and L² are as hereinbefore defined, for example at between 0° C. and reflux temperature in the presence of a suitable base (e.g. sodium hydroxide), an appropriate solvent (e.g. dichloromethane, water, or a mixture thereof) and, if necessary, a phase transfer catalyst (such as tetrabutylammonium hydrogensulfate).

Compounds of formula VIIIA and VIIIB may be prepared in a similar fashion to compounds of formula I (see, for example process steps (a) to (d)).

Compounds of formula XIIA and XIIB may be prepared by replacement of the —OH group of a corresponding compound of formula I in which R⁴ represents —OH with an L² group under conditions that are known to those skilled in the art.

Compounds of formula XIIIA and XIIIB in which E represents a direct bond may be prepared by reaction of corresponding compounds of formula I in which R⁴ represents —OH with a compound of formula XXXIV,

R³³S(O)₂Cl  XXXIV

wherein R³³ represents C₁₋₄ alkyl or aryl (which two groups are optionally substituted by one or more substituents selected from C₁₋₄ alkyl, halo and nitro), for example at between −10 and 25° C. in the presence of a suitable solvent (e.g. dichloromethane), followed by reaction with a suitable source of the azide ion (e.g. sodium azide), for example at between ambient and reflux temperature in the presence of an appropriate solvent (e.g. N,N-dimethylformamide) and a suitable base (e.g. sodium hydrogencarbonate).

Compounds of formula XIIIA and XlIIB may alternatively be prepared by reaction of a compound of formula IIA or IIB, as hereinbefore defined (except that R¹ or R² (as appropriate) does not represent a fragment of formula Ia), with a compound of formula XXXV,

wherein R⁵, R⁶, A, B, E, G and L² are as hereinbefore defined, for example under analogous conditions to those described hereinbefore for the synthesis of compounds of formula I (process step (a)).

Compounds of formula XVIIIA and XVIIIB may be prepared by removing an optionally substituted benzyloxycarbonyl unit from (i.e. deprotecting) corresponding compounds of formula I in which B represents —N(R²⁵)C(O)OCH₂— and A represents J, wherein R²⁵ and J are as hereinbefore defined, for example under conditions which are known to those skilled in the art.

Compounds of formula XXI may be prepared by reaction of a compound of formula m in which R²⁸ represents a fragment of formula Ia with a compound of formula XXXVI,

wherein R^(a) to R^(h) are as hereinbefore defined, for example under conditions described hereinbefore (process step (a)).

Compounds of formula XXI in which both R^(a) and R^(b) represent H may alternatively be prepared by reaction of a compound of formula XXXVII,

wherein R^(c) to R^(h) are as hereinbefore defined, with a compound of formula XXXVIII,

wherein R⁴, R⁵, R⁶, A, B and G are as hereinbefore defined, in the presence of a formaldehyde (i.e. an appropriate source of formaldehyde, such as paraformaldehyde or formalin solution), for example at between room and reflux temperature in the presence of a suitable solvent (e.g. a lower alkyl alcohol such as methanol) and optionally in the presence of an appropriate acid (e.g. acetic acid).

Compounds of formula XXV may be prepared by reaction of a compound of formula XXXVI, as hereinbefore defined, or a N-protected derivative thereof, with a compound of formula XXXIX,

R³—NH₂  XXXIX

or (in the case where R³ represents H) a protected derivative (e.g. N-benzyl) thereof, for example under conditions described hereinbefore for the synthesis of compounds of formula I (process step (s)).

Compounds of formula XXXV may be prepared in analogous fashion to compounds of formula XIIIA and XIIIB (i.e. from the corresponding alcohol).

Compounds of formula XXXVI in which both R^(a) and R^(b) represent H may be prepared by reaction of a compound of formula XXXVII with ammonia, or an N-protected derivative thereof (e.g. benzylamine), in the presence of a formaldehyde, for example under conditions described hereinbefore for the synthesis of compounds of formula XX.

Compounds of formulae V, VI, IX, X, XI, XIV, XV, XVI, XVII, XIX, XX, XXII, XXIII, XXV, XXVI, XXVII, XXVIII, XXIX, XXX, XXXIA, XXXIB, XXXIIA, XXXIIB, XXXIII, XXXIV, XXXVII, XXXVIII and XXXIX, and derivatives thereof, are either commercially available, are known in the literature, or may be obtained either by analogy with the processes described herein, or by conventional synthetic procedures, in accordance with standard techniques, from readily available starting materials using appropriate reagents and reaction conditions.

Substituents on the aryl (e.g. phenyl), and (if appropriate) heterocyclic, group(s) in compounds defined herein may be converted to other claimed substituents using techniques well known to those skilled in the art. For example, hydroxy may be converted to alkoxy, phenyl may be halogenated to give halophenyl, nitro may be reduced to give amino, amino may be acetylated to give acetylamino, etc.

The skilled person will also appreciate that various standard substituent or functional group interconversions and transformations within certain compounds of formula I will provide other compounds of formulae I. For example, carbonyl may be reduced to hydroxy or alkylene, and hydroxy may be converted to halo.

The compounds of the invention may be isolated from their reaction mixtures using conventional techniques.

It will be appreciated by those skilled in the art that, in the process described above, the functional groups of intermediate compounds may be, or may need to be, protected by protecting groups.

Functional groups which it is desirable to protect include hydroxy, amino and carboxylic acid. Suitable protecting groups for hydroxy include trialkylsilyl and diarylalkylsilyl groups (e.g. tert-butyldimethylsilyl, tert-butyldiphenylsilyl or trimethylsilyl), tetrahydropyranyl and alkylcarbonyl groups (e.g. methyl- and ethylcarbonyl groups). Suitable protecting groups for amino include benzyl, tert-butyloxycarbonyl, 9-fluorenyl-methoxycarbonyl or benzyloxycarbonyl. Suitable protecting groups for amidino and guanidino include benzyloxycarbonyl. Suitable protecting groups for carboxylic acid include C₁₋₆ alkyl or benzyl esters.

The protection and deprotection of functional groups may take place before or after any of the reaction steps described hereinbefore.

Protecting groups may be removed in accordance with techniques which are well known to those skilled in the art and as described hereinafter.

The use of protecting groups is fully described in “Protective Groups in Organic Chemistry”, edited by J. W. F. McOmie, Plenum Press (1973), and “Protective Groups in Organic Synthesis”, 3^(rd) edition, T. W. Greene & P. G. M. Wutz, Wiley-Interscience (1999).

Persons skilled in the art will appreciate that, in order to obtain compounds of the invention in an alternative, and, on some occasions, more convenient, manner, the individual process steps mentioned herein may be performed in a different order, and/or the individual reactions may be performed at a different stage in the overall route (i.e. substituents may be added to and/or chemical transformations performed upon, different intermediates to those associated hereinbefore with a particular reaction). This will depend inter alia on factors such as the nature of other functional groups present in a particular substrate, the availability of key intermediates and the protecting group strategy (if any) to be adopted. Clearly, the type of chemistry involved will influence the choice of reagent that is used in the said synthetic steps, the need, and type, of protecting groups that are employed, and the sequence for accomplishing the synthesis.

It will also be appreciated by those skilled in the art that, although certain protected derivatives of compounds of formula I, which may be made prior to a final deprotection stage, may not possess pharmacological activity as such, they may be administered parenterally or orally and thereafter metabolised in the body to form compounds of the invention which are pharmacologically active. Such derivatives may therefore be described as “prodrugs”. Moreover, certain compounds of formula I may act as prodrugs of other compounds of formula I.

All prodrugs of compounds of formula I are included within the scope of the invention.

Some of the intermediates referred to hereinbefore are novel. According to a further aspect of the invention there is thus provided: (a) a compound of formula IIA or IIB, as hereinbefore defined, or a protected derivative thereof; (b) a compound of formula IVA or IVB, as hereinbefore defined, or a protected derivative thereof; (c) a compound of formula VIIIA or VIIIB, as hereinbefore defined, or a protected derivative thereof; (d) a compound of formula XIIA or XIIB, as hereinbefore defined, or a protected derivative thereof; (e) a compound of formula XIIIA or XIIIB, as hereinbefore defined, or a protected derivative thereof; (t) a compound of formula XVIIIA or XVIIIB, as hereinbefore defined, or a protected derivative thereof; (g) a compound of formula XX, as hereinbefore defined (provided that when R^(a) to R^(h) all represent H, G represents CH and R⁶ is absent, then the group —A—C(R⁴)(R⁵)—B— does not represent unsubstituted ethyl), or a protected derivative thereof; and (h) a compound of formula XXIV, as hereinbefore defined (provided that R^(a) to R^(h) do not all represent H), or a protected derivative thereof.

Compounds of formula IIA that may be mentioned include those in which when R³ represents H and R² represents —C(O)R^(7a), then R^(7a) does not represent phenyl substituted in the 2-position by C₁₋₆ alkoxy, in the 4-position by —NH₂ or —N(H)C(O)R^(27h) (wherein R^(27h) represents C₁₋₆ alkyl), and in the 5-position by halo or —SR^(26c).

Compounds of formula IIB that may be mentioned include those in which:

(i) when R^(a) to R^(h) and R³ all represent H then R¹ does not represent C₁₋₃ alkyl optionally substituted by phenyl;

(ii) when R³ represents H then R¹ does not represent C₁₋₁₀ alkyl, or C₁₋₂ alkyl terminated by phenyl or thienyl (which phenyl or thienyl group is optionally substituted by one or two substituents selected from C₁₋₆ alkyl (optionally interrupted by oxygen), C₁₋₄ alkoxy, CF₃, halo, nitro, —C(O)OH or —C(O)O—C₁₋₆ alkyl;

(iii) R¹ does not represent C₁₋₂ alkyl substituted by phenyl (which phenyl group bears a para-[2-amino4-(C₁₋₆ alkyl)-pyridin-6-yl] substituent and optionally one or two further substituents independently selected from methyl, methoxy and hydroxy) and optionally by one or two further aryl groups;

(iv) R¹ does not represent C₂ alkyl terminated by phenyl (which phenyl group bears a para-{2-[1-(2,5-dimethyl-1H-pyrrolyl)-4(C₁₋₆ alkyl)-pyridin-6-yl} substituent and optionally one or two further substituents independently selected from methyl, methoxy and hydroxy); or

(v) R¹ does not represent C₁ alkyl substituted by phenyl (which phenyl group bears a para-{2-[N-phthaloyl]4-(C₁₋₆ alkyl)-pyridin-6-yl} substituent and a meta-methyl, methoxy or hydroxy group).

Medical and Pharmaceutical Use

The compounds of the invention are useful because they possess pharmacological activity. They are therefore indicated as pharmaceuticals.

Thus, according to a further aspect of the invention there is provided the compounds of the invention for use as pharmaceuticals.

In particular, the compounds of the invention exhibit myocardial electrophysiological activity, for example as demonstrated in the test described below.

The compounds of the invention are thus expected to be useful in both the prophylaxis and the treatment of arrhythmias, and in particular atrial and ventricular arrhythmias.

The compounds of the invention are thus indicated in the treatment or prophylaxis of cardiac diseases, or in indications related to cardiac diseases, in which arrhythmias are believed to play a major role, including ischaemic heart disease, sudden heart attack, myocardial infarction, heart failure, cardiac surgery and thromboembolic events.

In the treatment of arrhythmias, compounds of the invention have been found to selectively delay cardiac repolarization, thus prolonging the QT interval, and, in particular, to exhibit class III activity. Although compounds of the invention have been found to exhibit class III activity in particular, in the treatment of arrhythmias, their mode(s) of activity is/are not necessarily restricted to this class.

According to a further aspect of the invention, there is provided a method of treatment of an arrhythmia which method comprises administration of a therapeutically effective amount of a compound of the invention to a person suffering from, or susceptible to, such a condition.

Pharmaceutical Preparations

The compounds of the invention will normally be administered orally, subcutaneously, intravenously, intraarterially, transdermally, intranasally, by inhalation, or by any other parenteral route, in the form of pharmaceutical preparations comprising the active ingredient either as a free base, a pharmaceutically acceptable ion exchanger or a non-toxic organic or inorganic acid addition salt, in a pharmaceutically acceptable dosage form. Depending upon the disorder and patient to be treated, as well as the route of administration, the compositions may be administered at varying doses.

The compounds of the invention may also be combined with any other drugs useful in the treatment of arrhythmias and/or other cardiovascular disorders.

According to a further aspect of the invention there is thus provided a pharmaceutical formulation including a compound of the invention in admixture with a pharmaceutically acceptable adjuvant, diluent or carrier.

Suitable daily doses of the compounds of the invention in therapeutic treatment of humans are about 0.005 to 10.0 mg/kg body weight at oral administration and about 0.005 to 5.0 mg/kg body weight at parenteral administration.

The compounds of the invention have the advantage that they are effective against cardiac arrhythmias.

Compounds of the invention may also have the advantage that they may be more efficacious than, be less toxic than, have a broader range of activity (including exhibiting any combination of class I, class II, class III and/or class IV activity (especially class I and/or class IV activity in addition to class III activity)) than, be more potent than, be longer acting than, produce fewer side effects (including a lower incidence of proarrhythmias such as torsades de pointes) than, be more easily absorbed than, or that they may have other useful pharmacological properties over, compounds known in the prior art.

Biological Tests

Test A

Glucocorticoid-treated Mouse Fibroblasts as a Model to Detect Blockers of the Delayed Rectifier K Current

IC50 for K channel blockade was determined using a microtitre plate based screen method, based on membrane potential changes of glucocorticoid-treated mouse fibroblasts. The membrane potential of glucocorticoid-treated mouse fibroblasts was measured using fluorescence of the bisoxonol dye DiBac₄₍₃₎, which could be reliably detected using a fluorescence laser imaging plate reader (FLIPR). Expression of a delayed rectifier potassium channel was induced in mouse fibroblasts by 24 hours exposure to the glucocorticoide dexamehasone (5 μM). Blockade of these potassium channels depolarised the fibroblasts, resulting in increased fluorescence of DiBac₄₍₃₎.

Mouse ltk fibroblasts (L-cells) were purchased from American Type Culture Collection (ATCC, Manassa, Va.), and were cultured in Dulbeccos modified eagle medium supplemented with fetal calf serum (5% vol/vol), penicillin (500 units/mL), streptomycin (500 μg/mL) and L-alanine-L-glutamine (0.862 mg/mL). The cells were passaged every 3-4 days using trypsin (0.5 mg/mL in calcium-free phosphate buffered saline, Gibco BRL). Three days prior to experiments, cell-suspension was pipetted out into clear-bottom, black plastic, 96-well plates (Costar) at 25 000 cells/well.

The fluorescence probe DiBac₄₍₃₎ ₍DiBac Molecular probes) was used to measure membrane potential. DiBac₄₍₃₎ maximally absorbs at 488 nM and emits at 513 nM. DiBac₄₍₃₎ is a bisoxonol, and thus is negatively charged at pH 7. Due to its negative charge, the distribution of DiBac₄₍₃₎ across the membrane is dependent upon the transmembrane potential: if the cell depolarizes (i.e. the cell interior becomes less negative relative to cell exterior), the DiBac₄₍₃₎ concentration inside the cell increases, due to electrostatic forces. Once inside the cell, DiBac₄₍₃₎ molecules can bind to lipids and proteins, which causes an increase in fluorescence emission. Thus, a depolarization will be reflected by an increase in DiBac₄₍₃₎ fluorescence. The change in DiBac₄₍₃₎ fluorescence was detected by a FLIPR.

Prior to each experiment, the cells were washed 4 times in phosphate-buffered saline (PBS) to remove all culture media. The cells were then treated with 5 μM DiBac₄₍₃₎ (in 180 μL of PBS) at 35° C. Once a stable fluorescence was reached (usually after 10 min), 20 μL of the test substance was added, using FLIPR's internal 96 well pipetting system. Fluorescence measurements were then taken every 20 sec for a further 10 min. All experiments were carried out at 35° C., due to the high temperature sensitivity of both delayed rectifier potassium channel conductance and DiBac₄₍₃₎ fluorescence. Test substances were prepared in a second 96 well plate, in. PBS containing 5 μM DiBac₄₍₃₎. The concentration of substance prepared was 10 times that of the desired concentration in the experiment as an additional 1:10 dilution occurred during addition of substance during the experiment. Dofetilide (10 μM) was used as a positive control, i.e. to determine the maximum increase in fluorescence.

Curve-fitting, used to determine the IC50 values, was performed with the Graphpad Prism program (Graphpad Software Inc., San Diego, Calif.).

Test B

Metabolic Stability of Test Compounds

An in vitro screen was set up to determine the metabolic stability of the compounds of the invention.

The hepatic S-9 fraction from dog, man, rabbit and rat with NADPH as co-factor was used. The assay conditions were as follows: S-9 (3 mg/mL), NADPH (0.83 mM), Tris-HCl buffer (50 mM) at pH 7.4 and 10 μM of test compound.

The reaction was started by addition of test compound and terminated after 0, 1, 5, 15 and 30 minutes by raising the pH in the sample to above 10 (NaOH; 1 mM). After solvent extraction, the concentration of test compound was measured against an internal standard by LC (fluorescence/UV detection).

The percentage of test compound remaining after 30 minutes (and thus t_(½)) was calculated and used as a measure for metabolic stability.

The invention is illustrated by way of the following examples.

EXAMPLES General Experimental Procedures

Mass spectra were recorded on one of the following instruments: a Perkin-Elmer SciX API 150ex spectrometer; a VG Quattro II triple quadrupole; a VG Platform II single quadrupole; or a Micromass Platform LCZ single quadrupole mass spectrometer (the latter three instruments were equipped with a pneumatically assisted electrospray interface (LC-MS)). ¹H NMR and ¹³C NMR measurements were performed on a BRUKER ACP 300 and Varian 300, 400 and 500 spectrometers, operating at ¹H frequencies of 300, 400 and 500 MHz respectively, and at ¹³C frequencies of 75.5, 100.6 and 125.7 MHz respectively. Alternatively, ¹³C NMR measurements were performed on a BRUKER ACE 200 spectrometer at a frequency of 50.3 MHz.

Rotamers may or may not be denoted in spectra depending upon ease of interpretation of spectra. Unless otherwise stated, chemical shifts are given in ppm with the solvent as internal standard.

Synthesis of Intermediates

The following intermediates were not commercially available, and were therefore prepared by the methods described below.

Preparation A 3-Benzyl-3-azabicyclo[3.2.1]octan-8-one

A solution of benzylamine (127.4 g, 1.19 mol) in methanol (125 mL) was added dropwise over 3 h to a refluxing solution of cyclopentanone (100 g, 1.19 mol), paraformaldehyde (107 g, 3.57 mol), and glacial acetic acid (71.4 g, 1.19 mol) in methanol (600 mL) under nitrogen. After 1 h at reflux, the brown mixture was stirred overnight at 25° C. and concentrated in vacuo. The resulting oil was diluted with water (200 mL) and basified with 6 N NaOH (200 mL). The aqueous solution was extracted with dichloromethane (3×400 mL). The combined organic extracts were dried (Na₂SO₄), and concentrated in vacuo. The residue was chromatographed, eluting with ethyl acetate: dichloromethane (1:35), to afford 47.6 g (19%) of the sub-title compound as a yellow oil.

¹H NMR (300 MHz, CCDl₃): δ 7.40-7.10 (m, 5H), 3.60 (s, 2H), 3.01-2.92 (m, 2 H), 2.57-2.50 (m, 2H), 2.18-2.0 (m, 4H), 1.90-1.81 (m, 2H).

Preparation B 3-Benzyl-N-methyl-3-azabicyclo[3.2.1]octan-8-amine

A mixture of sodium cyanoborohydride (35.0 g, 0.557 mol) and zinc chloride (37.9 g, 0.278 mol) in methanol (500 mL) was added dropwise to a mechanically stirred mixture of 3-benzyl-3-azabicyclo[3.2.1]octan-8-one (Preparation A; 120 g, 0.557 mol) and methylamine hydrochloride (151 g, 2.23 mol) in methanol (1.0 L) at 25° C. under nitrogen. After 2.5 h of stirring, 6 N NaOH (90 mL) was added dropwise. The mixture was filtered through a pad of Celite®, washing with methanol (500 mL). The filtrate was concentrated in vacuo. Water (500 mL) was added, and the aqueous mixture was extracted with ethyl acetate (3×500 mL). The combined organic extracts were dried (Na₂SO₄), and concentrated in vacuo. The residue was chromatographed, eluting with methanol dichloromethane (1:10), to afford 63.0 g (49%) of the sub-title compound as a solid.

¹H NMR (300 MHz, CCDl₃): δ 7.40-7.10 (m, 5H), 3.88 (s, 2H), 3.60 (s, 2H), 3.45 (s, 1H), 2.85-2.80 (m, 1H), 2.60-2.45 (m, 2H), 2.50 (s, 3H), 2.15 (s, 2H), 2.40-2.30 (m, 2H), 1.70-1.62 (m, 2H).

Preparation C tert-Butyl 3-Benzyl-3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate

A mixture of 3-benzyl-N-methyl-3-azabicyclo[3.2.1]octan-8-amine (Preparation B; 168.1 g, 0.730 mol) and di-tert-butyldicarbonate (159 g, 0.730 mol) in dichloromethane (2.5 L) was stirred overnight at 25° C. under nitrogen. The mixture was concentrated in vacuo to yield 240 g (100%) of the sub-title compound as a white solid, which was used without purification.

¹H NMR (300 MHz, CCDl₃): δ 7.40-7.30 (m, 5H), 4.0 (s, 2H), 3.60 (s, 2H), 3.45 (s, 1H), 3.02-2.50 (m, 5H), 2.80 (s, 3H), 2.0-1.70 (m, 4H), 1.50 (s, 9H).

Preparation D tert-Butyl 3-Azabicyclo[3.2.1]oct-8-yl(methyl)carbamate

A solution of 1 M HCl in diethyl ether (730 mL, 730 mmol) was added dropwise to a solution tert-butyl 3-benzyl-3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate (Preparation C; 241 g, 0.730 mol) in diethyl ether (1.5 L). The resulting precipitate was collected via filtration through a sintered glass funnel and then dried in vacuo. The solid was dissolved in methanol (4.0 L), and 10% palladium on carbon (24 g) was added. The mixture was stirred under one atmosphere of hydrogen at 40° C. overnight. The catalyst was filtered through a pad of Celite®, washing with methanol (1.0 L). The filtrate was concentrated in vacuo, and chromatographed, eluting with dichloromethane:methanol:concentrated ammonium hydroxide (88:10:2) to afford 70 g (40%) of an oil. A solution of this oil (70 g, 296 mmol) in diethyl ether (1.0 L) was treated with 1 M HCl in diethyl ether (300 mL), added dropwise. The resulting precipitate was removed via filtration through sintered glass funnel. The salt was slurried in acetonitrile and the solid collected to give 80 g of the HCl salt of the title compound:

Mp: 170-177° C.; ¹H NMR (300 MHz, CD₃OD): δ 3.35-3.10 (m, 6H), 2.90 (s, 3H), 3.02-2.80 (m, 2H), 2.02-1.70 (m, 4H), 1.45 (s, 9H). ¹³C NMR (75 MHz, CD₃OD): δ 159.2, 81.8, 61.6, 45.6, 36.6, 36.0, 28.5, 24.8. CI-MS: (M+1)=241 m/z.

The free base was obtained by treating the HCl salt with K₂CO₃ in MeCN

Preparation E 4-{3-[3-Azabicyclo[3.2.1]oct-8-yl(methyl)amino]-2-hydroxypropoxy}-benzonitrile

(i) 4-(2-Oxiranylmethoxy)benzonitrile

Epichlorohydrin (800 mL) and K₂CO₃ (414 g) were added to a stirred solution of p-cyanophenol (238 g) in 2.0 L MeCN and the reaction mixture was refluxed under inert atmosphere for 2 h. The hot solution was filtered and the filtrate concentrated to give a clear oil. This was crystallized from di-iso-propyl ether to give the sub-title compound in 75% yield.

(ii) 4-{3-[(3-Benzyl-3-azabicyclo[3.2.1]oct-8-yl)(methyl)amino]-2-hydroxypropoxy}benzonitrile

To a solution of 3-benzyl-N-methyl-3-azabicyclo[3.2.1]octan-8-amine (Preparation B; 3.72 g, 16.1 mmol) in dichloromethane (80 mL) at 25° C. under nitrogen was added trimethylaluminum (8.05 mL of 2.0 M in hexane, 16.1 mmol). After stirring at 25° C. for 30 min, 4-(2-oxiranyl-methoxy)benzonitrile (see step (i) above; 2.83 g, 16.1 mmol) was added in one portion, and the mixture was stirred overnight. The mixture was quenched with 6 N NaOH (13.5 mL) and stirred 1 h. Water (100 mL) was added, and the aqueous layer was extracted with dichloromethane (3×100 mL). The combined organic extracts were dried (Na₂SO₄), filtered and concentrated in vacuo to afford an oil. The residue was chromatographed on silica gel, eluting with dichloromethane:methanol (98:2), to afford 4.30 g (66%) of the sub-title compound as a colorless oil.

¹H NMR (300 MHz, CDCl₃): δ 7.58 (d, J=8.2 Hz, 2H), 7.32-7.20 (m, 5H), 6.97 (d, J=8.2 Hz, 2H), 4.22-4.14 (m, 1H), 4.08-4.0 (m, 2H), 3.50 (s, 2H), 2.82-2.70 (m, 1H), 2.64-2.52 (m, 2H), 2.48-2.30 (m, 5H), 2.30 (s, 3H), 1.94-1.82 (m, 2H), 1.72-1.50 (m, 4H). ¹³C NMR (75 MHz, CDCl₃): δ 162.4, 139.4, 134.0, 128.2, 128.0, 126.8, 119.5, 115.6, 104.4, 70.6, 68.0, 66.0, 62.4, 57.7, 52.4, 52.0, 40.4, 36.8, 36.2, 27.8. CI-MS: (M+1)=406 m/z.

(iii) 4-{3-[3-Azabicyclo[3.2.1]oct-8-yl(methyl)amino]-2-hydroxypropoxy}-benzonitrile

A solution of HCl in ether (4.3 mL of 1.0 M, 4.3 mmol) was added dropwise to a solution of 4-{3-[(3-benzyl-3-azabicyclo[3.2.1]oct-8-yl)(methyl)amino]-2-hydroxypropoxy}benzonitrile (see step (ii) above; 1.75 g, 4.32 mmol) in diethyl ether (50 mL) at 0° C. Concentration in vacuo gave the HCl salt. The HCl salt and 10% palladium on carbon (175 mg) were suspended in methanol (25 mL), then stirred under an atmosphere of hydrogen for 5 h at 40° C. The catalyst was removed by filtration through a short pad of Celite®, washing with methanol (50 mL). The filtrate was concentrated in vacuo and chromatographed on silica gel, eluting with dichloromethane:methanol:concentrated ammonium hydroxide (88:10:2), to afford 980 mg (72%) of the tide compound as a white foam.

¹H NMR (300 MHz, CDCl₃): δ 7.58 (d, J=8.2 Hz, 2H), 6.97 (d, J=8.2 Hz, 2H), 4.30-4.16 (m, 1H), 4.12-4.0 (m, 2H), 3.33-3.10 (m, 4H), 2.82-2.70 (m, 1H), 2.52-2.30 (m, 4H), 2.30 (s, 3H), 2.20-2.05 (m, 2H), 1.91-1.70 (m, 4H). ¹³C NMR (75 MHz, CDCl₃): δ 162.4, 134.0, 119.5, 115.6, 104.4, 70.6, 68.0, 66.0, 57.7, 52.0, 40.4, 36.8, 36.2, 27.8. CI-MS: (M+1)=316 m/z.

Preparation F 4-{2-Hydroxy-3-[8-(methylamino)-3-azabicyclo[3.2.1]oct-3-yl]propoxy}-benzonitrile

(i) tert-Butyl 3-[3-(4-Cyanophenoxy)-2-hydroxypropyl]-3-azabicyclo-[3.2.1]oct-8-yl(methyl)carbamate

To a solution of tert-butyl 3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate (Preparation D; 1.68 g, 7.0 mmol) in dichloromethane (35 mL) at 25° C. under nitrogen was added trimethylaluminum (3.75 mL of 2.0 M in hexanes, 7.0 mmol). After stirring at 25° C. for 30 min, 4-(2-oxiranyl-methoxy)benzonitrile (Preparation E(i); 1.22 g, 7.0 mmol) was added in one portion, and the mixture was stirred overnight. The mixture was quenched with 3 N NaOH (11.5 mL) and stirred for 1 h. Water (30 mL) was added, and the aqueous layer was extracted with dichloromethane (3×30 mL). The combined organic extracts were dried (Na₂SO₄), filtered and concentrated in vacuo to afford an oil. The residue was chromatographed on silica gel, eluting with dichloromethane:methanol (98:2), to afford 2.35 g (81%) of the subtitle compound as a white solid.

Mp: 109-112° C.; ¹H NMR (300 MHz, CDCl₃): δ 7.58 (d, J=8.2 Hz, 2H), 6.97 (d, J=8.2 Hz, 2H), 4.10-3.70 (m, 3H), 3.22-3.16 (m, 1H), 2.90 (s, 3H), 2.70-2.25 (m, 8H), 1.50-1.82 (m, 5H), 1.45 (s, 9H). ¹³C NMR (75 MHz, CDCl₃): δ 162.2, 157.6, 134.0, 132.7, 119.2, 115.6, 104.1, 79.8, 70.6, 65.2, 60.8, 59.8, 58.0, 55.2, 52.0, 37.8, 37.2, 35.4, 28.4, 26.1, 26.0. CI-MS: (M+1)=416 m/z.

(ii) 4-[2-Hydroxy-3-[8-(methylamino)-3-azabicyclo[3.2.1]oct-3-yl]-propoxy}benzonitrile

A suspension of tert-butyl 3-[3-(4-cyanophenoxy)-2-hydroxypropyl]-3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate (see step (i) above; 3.15 g, 7.58 mmol) in ethyl acetate saturated with HCl (40 mL) was stirred for 5 h at 25° C. under nitrogen. The mixture was partitioned with water (100 mL) and ethyl acetate (50 mL). The aqueous layer was separated and washed with ethyl acetate. The aqueous layer was separated, basified with saturated sodium bicarbonate (30 mL) and then extracted with dichloromethane (3×50 mL). The organic extracts were dried (Na₂SO₄), filtered, concentrated in vacuo and then chromatographed on silica gel, eluting with dichloromethane:methanol:concentrated ammonium hydroxide (88:10:2), to afford 2.30 g (96%) of the title compound as a colorless oil.

¹H NMR (300 MHz, CDCl₃): δ 7.58 (d, J=8.2 Hz, 2H), 6.97 (d, J=8.2 Hz, 2H), 4.10-3.90 (m, 4H), 3.90 (d, J=8.2 Hz, 1H), 2.70-2.67 (m, 1H), 2.60-2.30 (m, 5H), 2.40 (s, 3H), 2.08-2.0 (m, 2H), 1.82-1.64 (m, 5H). ¹³C NMR (75 MHz, CDCl₃): δ 162.2, 134.0, 132.7, 119.2, 115.6, 104.1, 70.6, 65.2, 60.8, 59.8, 54.2, 50.4, 37.8, 37.2, 35.4, 27.4, 27.2. CI-MS: (M+1)=316 m/z.

Preparation G 4-({3-[8-(Methylamino)-3-azabicyclo[3.2.1]oct-3-yl]propyl}amino)-benzonitrile

(i) 4-[(3-Hydroxypropyl)amino]benzonitrile

A mixture of 4-fluorobenzonitrile (12.0 g, 99.1 mmol) and 3-amino-1-propanol (59.6 g, 793 mmol) was stirred at 80° C. under an inert atmosphere for 3 hours before water (150 mL) was added. The mixture was allowed to cool to rt, and was then extracted with diethyl ether. The organic layer was separated, dried (Na₂SO₄), filtered and concentrated in vacuo to yield 17 g (97%) of the title compound as an oil that crystallised upon standing.

(ii) 3-(4-Cyanoanilino)propyl 4-Methylbenzenesulfonate

A cooled (0° C.) solution of 4-[(3-hydroxypropyl)amino]benzonitrile (see step (i) above; 17 g, 96.5 mmol) in dry MeCN (195 mL) was treated with triethylamine (9.8 g, 96.5 mmol) and then p-toluenesulfonyl chloride (20.2 g, 106 mmol). The mixture was stirred at 0° C. for 90 minutes before being concentrated in vacuo. Water (200 mL) was added to the residue, and the aqueous solution was extracted with DCM. The organic phase was dried (Na₂SO₄), filtered and concentrated in vacuo. The resulting residue was purified by crystallisation from iso-propanol to yield 24.6 g (77%) of the sub-title compound.

(iii) tert-Butyl 3-[3-(4-Cyanoanilino)propyl]-3-azabicyclo[3.2.1]oct-8-yl-(methyl)carbamate

A mixture of tert-butyl 3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate (Preparation D; 2.90 g, 12.1 mmol), 3-(4-cyanoanilino)propyl 4-methyl-benzenesulfonate (see step (ii) above; 3.98 g, 12.1 mmol), and potassium carbonate (1.67 g, 12.1 mmol) in DMF (50 mL) was heated at 90° C. under nitrogen for 4 h. The mixture was partitioned with water (50 mL) and diethyl ether (50 mL). The aqueous layer was separated and then extracted with diethyl ether (2×50 mL). The combined organic extracts were washed with saturated brine (2×30 mL), dried (Na₂SO₄), filtered and then concentrated in vacuo. The residue was chromatographed on silica gel, eluting with dichloromethane:methanol (98:2), to afford 2.85 g (59%) of the sub-title compound.

¹H NMR (300 MHz, CDCl₃): δ 7.40 (d, J=8.2 Hz, 2H), 6.52 (d, J=8.2 Hz, 2H), 3.25-3.18 (m, 4H), 2.80 (s, 3H), 2.72-2.60 (m, 4H), 2.50-2.42 (m, 2H), 2.28-2.20 (m, 2H), 1.85-1.70 (m, 6H), 1.45 (s, 9H). ¹³C NMR (75 MHz, CDCl₃): δ 157.4, 152.0, 133.8, 133.2, 120.4, 111.8, 97.7, 79.8, 61.4, 57.8, 53.9, 44.2, 37.8, 35.0, 28.0, 26.0, 24.2. CI-MS: (M+1)=399 m/z.

(iv) 4-({3-[8-(Methylamino)-3-azabicyclo[3.2.1]oct-3-yl]propyl}amino)-benzonitrile

A suspension of tert-butyl 3-[3-(4-cyanoanilino)propyl]-3-azabicyclo-[3.2.1]oct-8-yl(methyl)carbamate (see step (iii) above; 2.66 g, 6.67 mmol) in ethyl acetate saturated with HCl (40 mL) was stirred overnight at 25° C. under nitrogen. The mixture was partitioned with water (100 mL) and ethyl acetate (50 mL). The aqueous layer was basified with saturated sodium bicarbonate (50 mL) and then extracted with dichloromethane (3×50 mL). The organic extracts were dried (Na₂SO₄), filtered, concentrated in vacuo and then chromatographed on silica gel, eluting with dichloromethane:methanol:concentrated ammonium hydroxide (92:7:1), to afford 1.07 g (54%) of the title compound as a white solid.

¹H NMR (300 MHz, CD₃OD): δ 7.40 (d, J=8.2 Hz, 2H), 6.52 (d, J=8.2 Hz, 2H), 3.40-3.10 (m, 6H), 2.72-2.40 (m, 6H), 2.40 (s, 3H), 2.22-2.0 (m, 2H), 1.80-1.62 (m, 5H). ¹³C NMR (75 MHz, CD₃OD): δ 154.0, 134.2, 113.4, 97.7, 64.4, 57.8, 53.9, 42.5, 37.8, 34.0, 28.0, 26.0. CI-MS: (M+1)=299 m/z.

Preparation H 4-({3-[3-Azabicyclo[3.2.1]oct-8-yl(methyl)amino]propyl}amino)-benzonitrile

(i) 4-(13-[(3-Benzyl-3-azabicyclo[3.2.1]oct-8-yl)(methyl)amino]propyl]-amino)benzonitrile

A mixture of 3-benzyl-N-methyl-3-azabicyclo[3.2.1]octan-8-amine (Preparation B; 4.0 g, 17.4 mmol), 3-(4-cyanoanilino)propyl 4-methyl-benzenesulfonate (Preparation G(ii); 5.74 g, 17.4 mmol), and potassium carbonate (2.40 g, 17.4 mmol) in DMF (85 mL) was heated at 90° C. under nitrogen overnight. The mixture was partitioned with water (200 mL) and diethyl ether (150 mL). The aqueous layer was extracted with ethyl acetate (2×50 mL). The combined organic extracts were washed with brine (2×30 mL), dried (Na₂SO₄), filtered and then concentrated in vacuo. The residue was chromatographed on silica gel, eluting with dichloromethane:methanol (98:2), to afford 3.40 g (50%) of the sub-title compound as a white solid.

Mp: 91-93° C.; ¹H NMR (300 MHz, CDCl₃): δ 7.48 (d, J=8.2 Hz, 2H), 7.32-7.20 (m, 5H), 6.60 (d, J=8.2 Hz, 2H), 5.78-5.70 (m, 1H), 3.50 (s, 2H), 3.30-3.20 (m, 2H), 2.62-2.52 (m, 4H), 2.40-2.32 (m, 2H), 2.25 (s, 3H), 2.25-2.10 (m, 3H), 1.92-1.80 (m, 4H), 1.72-1.60 (m, 2H). ¹³C NMR (75 MHz, CDCl₃): δ 152.2, 140.0, 133.8, 128.4, 128.2, 136.4, 121.2, 112.2, 98.4, 68.8, 62.4, 54.5, 52.8, 43.0, 39.9, 36.4, 28.8, 25.8. CI-MS: (M+1)=389 m/z.

(ii) 4-({3-[3-Azabicyclo[3.2.1]oct-8-yl(methyl)amino]propyl}amino)-benzonitrile

A solution of HCl in diethyl ether (3.4 mL of 1.0 M, 3.4 mmol) was added dropwise to a solution of 4-({3-[(3-benzyl-3-azabicyclo[3.2.1]oct-8-yl)(methyl)amino]propyl}amino)benzonitrile (see step (i) above; 1.32 g, 3.39 mmol) in diethyl ether (50 mL) at 0° C. Concentration in vacuo gave the HCl salt. The HCl salt and 10% palladium on carbon (132 mg) were suspended in methanol (20 mL) and stirred under an atmosphere of hydrogen for 2 h at 40° C. The catalyst was removed by filtration through a short pad of Celite®, washing with methanol (50 mL). The filtrate was concentrated in vacuo and chromatographed on silica gel, eluting with dichloromethane:methanol:concentrated ammonium hydroxide (88:10:2), to afford 590 mg (59%) of the title compound as a white foam.

Mp: 59-63° C.; ¹H NMR (300 MHz, CD₃OD): δ 7.48 (d, J=8.2 Hz, 2H), 6.66 (d, J=8.2 Hz, 2H), 4.80 (s, 1H), 3.35-3.10 (m, 4H), 2.62-2.40 (m, 4H), 2.30-2.10 (m, 4H), 2.25 (s, 3H), 1.91-1.70 (m, 6H). ¹³C NMR (75 MHz, CD₃OD): δ 154.0, 133.8, 122.2, 113.2, 97.8, 68.8, 54.5, 45.8, 42.0, 40.4, 37.0, 26.8, 26.6. CI-MS: (M+1)=299 m/z.

Preparation I 4-{1-(3,4-Dimethoxyphenoxy)-4-[8-(methylamino)-3-azabicyclo[3.2.1]oct-3-yl]butyl}benzonitrile

(i) 4-[1-(3,4-Dimethoxyphenoxy)-3-butenyl]benzonitrile

A cooled (0° C.) mixture of 4-(1-hydroxy-3-butenyl)benzonitrile (14.6 g, 84.3 mmol) and 3,4-dimethoxyphenol (19.5 g, 125.4 mmol) in toluene (500 mL) was treated with tributylphosphine (32.14 mL of 97% purity, 25.6 g, 126.4 mmol), followed by 1,1′-(azodicarbonyl)dipiperidine (31.8 g, 126.4 mmol). After addition was complete, the reaction mixture thickened and the temperature rose to 15° C. Additional toluene was added (500 mL), and the mixture stirred at rt overnight. The precipitate of tributylphosphine oxide was then removed by filtration and the filtrate concentrated in vacuo to give 65.8 g of crude product. This was purified by chromatography on silica gel, eluting with toluene:methanol (98:2), to yield 17.9 g of the sub-title compound.

(ii) 4-[1-(3,4-Dimethoxyphenoxy)-4-hydroxybutyl]benzonitrile

Borane-methyl sulfide complex (2 M in ether, 11 mL, 22 mmol) was added dropwise to a cooled (−5° C.) solution of 4-[1-(3,4-dimethoxyphenoxy)-3-butenyl]benzonitrile (see step (i) above; 17.6 g, 56.8 mmol) in dry THF (15 mL) over a period of 15 minutes (during which time the reaction temperature rose to 0° C.). The resulting mixture was stirred at between 0 and 10° C. for 1.5 h, before being allowed to warm to rt. Stirring was continued for a further 3.5 h at this temperature before water (22 mL) and sodium perborate tetrahydrate (11 g, 66 mmol) were added. The biphasic mixture was stirred for 2 h at rt before the water layer was separated and extracted with ether. The combined organic layers were washed with brine, dried and concentrated in vacuo. The resulting residue was purified by chromatography on silica gel, eluting with IPA: ethyl acetate:heptane (5:25:70) to yield 14.5 g (77%) of the sub-title compound.

(iii) 4-(4-Cyanophenyl)-4-(3,4-dimethoxyphenoxy)butyl Methanesulfonate

A solution of methanesulfonyl chloride (3.4 mL, 5.0 g, 44 mmol) in DCM (15 mL) was added slowly to a cooled (−5° C.) mixture of 4-[1-(3,4-dimethoxyphenoxy)-4-hydroxybutyl]benzonitrile (see step (ii) above; 11 g, 34 mmol) and triethylamine (7 mL, 5.2 g, 50.6 mmol) in DCM (50 ML), during which addition the temperature did not rise above 2° C. Stirring was continued at between 0 and 5° C. for a further 2 h before water was added. The resulting organic layer was separated, and washed with water, separated again and then dried to give the subtitle compound in 100% yield.

(iv) tert-Butyl 3-[4-(4-cyanophenyl)-4-(3,4-dimethoxyphenoxy)butyl]-3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate

A mixture of tert-butyl 3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate (Preparation D; 2.60 g, 10.9 mmol), 4-(4-cyanophenyl)-4-(3,4-dimethoxyphenoxy)butyl methanesulfonate (see step (iii) above; 4.40 g, 10.9 mmol), and potassium carbonate (1.50 g, 10.9 mmol) in DMF (50 mL) was heated at 90° C. under nitrogen for 4 h. The mixture was partitioned with water (50 mL) and diethyl ether (50 mL). The aqueous layer was extracted with diethyl ether (2×50 mL). The combined organic extracts were washed with brine (2×30 mL), dried (Na₂SO₄), filtered and then concentrated in vacuo. The residue was chromatographed on silica gel, eluting with dichloromethane:methanol (98:2), to afford 3.60 g (60%) of the sub-title compound as an amorphous solid.

¹H NMR (300 MHz, CDCl₃): δ 7.62 (d, J=8.2 Hz, 2H), 7.46 (d, J=8.2 Hz, 2H), 6.62 (d, J=8.2 Hz, 2H); 6.50 (s, 1H), 6.18 (d, J=4.0 Hz, 2H), 5.10 (m, 1H), 3.80 (s, 3H), 3.76 (s, 3H), 3.20-3.16 (m, 1H), 2.90 (s, 3H), 2.62-2.56 (m, 2H), 2.50-2.12 (m, 6H), 2.0-1.60 (m, 7H), 1.43 (s, 9H). 13C NMR (75 MHz, CDCl₃): δ 157.8, 152.0, 149.8, 148.2, 143.6, 132.4, 130.0, 118.4, 112.0, 111.7, 105.6, 102.2, 79.6, 79.4, 61.8, 57.6, 56.4, 55.8, 53.8, 53.4, 37.6, 35.8, 35.4, 28.2, 26.4, 22.4. CI-MS: (M+1)=550 m/z.

(v) 4-{1-(3,4-Dimethoxyphenoxy)-4-[8-(methylamino)-3-azabicyclo-[3.2.1]oct-3-yl]butyl}benzonitrile

A suspension of tert-butyl 3-[4-(4-cyanophenyl)-4-(3,4-dimethoxyphenoxy)butyl]-3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate (see step (iv) above; 2.67 g, 4.86 mmol) in ethyl acetate saturated with HCl (60 mL) was stirred overnight at 25° C. under nitrogen. The mixture was partitioned with water (100 mL) and ethyl acetate (50 mL). The aqueous layer was washed with ethyl acetate (50 mL) before being separated, basified with saturated sodium bicarbonate (50 mL) and then extracted with dichloromethane (3×50 mL). The organic extracts were dried (Na₂SO₄), filtered, concentrated in vacuo and then chromatographed on silica gel, eluting with dichloromethane:methanol:concentrated ammonium hydroxide (92:7:1), to afford 1.32 g (61%) of the title compound as a yellow oil.

¹H NMR (300 MHz, CDCl₃): δ 7.62 (d, J 8.2 Hz, 2H), 7.46 (d, J=8.2 Hz, 2H), 6.62 (d, J=8.2 Hz, 2H), 6.50 (s, 1H), 6.18 (d, J=4.0 Hz, 2H), 5.21-5.10 (m, 1H), 3.80 (s, 3H), 3.76 (s, 3H), 3.50-3.48 (m, 1H), 2.70-2.62 (m, 1H), 2.40 (s, 3H), 2.48-2.30 (m, 4H), 2.10-1.40 (m, 10H). ¹³C NMR (75 MHz, CDCl₃): δ 152.0, 149.8, 148.2, 143.6, 132.4, 126.5, 118.4, 112.0, 111.7, 105.6, 102.2, 79.6, 79.4, 62.5, 57.6, 56.4, 55.8, 53.8, 53.4, 37.6, 35.8, 35.4, 28.2, 26.4. CI-MS: (M+1)=450 m/z.

Preparation J 4-[4-[3-Azabicyclo[3.2.1]oct-8-yl(methyl)amino]-1-(3,4dimethoxyphenoxy)butyl]benzonitrile

(i) 4-[4-[(3-Benzyl-3-azabicyclo[3.2.1]oct-8-yl)(methyl)amino]-1-(3,4-dimethoxyphenoxy)butyl]benzonitrile

A mixture of 3-benzyl-N-methyl-3-azabicyclo[3.2.1]octan-8-amine (Preparation B; 1.3 g, 5.95 mmol), 4-(4-cyanophenyl)-4-(3,4-dimethoxyphenoxy)butyl methanesulfonate (Preparation I(iii); 2.41 g, 5.95 mmol), and potassium carbonate (822 mg, 5.95 mmol) in DMF (25 mL) was heated at 90° C. under nitrogen overnight. The mixture was partitioned with water (50 mL) and diethyl ether (40 mL). The aqueous layer was extracted with diethyl ether (2×40 mL). The combined organic extracts were washed with brine (2×30 mL), dried (Na₂SO₄), filtered and then concentrated in vacuo. The residue was chromatographed on silica gel, eluting with dichloromethane:methanol (98:2), to afford 860 mg (27%) of the sub-title compound.

¹H NMR (300 MHz, CDCl₃): δ 7.62 (d, J=8.2 Hz, 2H), 7.46 (d, J=8.2 Hz, 2H), 7.38-7.20 (m, 5H), 6.62 (d, J=8.2 Hz, 2H), 6.50 (s, 1H), 6.18 (d, J=4.0 Hz, 2H), 5.22-5.10 (m, 1H), 3.80 (s, 3H), 3.76 (s, 3H), 3.50 (s, 2H), 2.68-2.52 (m, 2H), 2.50-2.28 (m, 4H), 2.15 (s, 3H), 2.0-1.75 (m, 4H), 1.68-1.50 (m, 5H). ¹³C NMR (75 MHz, CDCl₃): δ 152.0, 149.8, 148.2, 143.6, 140.0, 132.4, 128.0, 127.8, 126.0, 118.4, 112.0, 111.7, 105.6, 102.2, 79.6, 68.4, 61.8, 59.2, 57.6, 56.4, 55.8, 53.8, 53.4, 39.8, 35.8, 35.4, 28.2, 22.4. CI-MS: (M+1)=540 m/z.

(ii) 4-[4-[3-Azabicyclo[3.2.1]oct-8-yl(methyl)amino]-1-(3,4dimethoxyphenoxy)butyl]benzonitrile

A solution of HCl in diethyl ether (4.1 mL of 1.0 M, 4.1 mmol) was added dropwise to a solution of 4-[4-[(3-benzyl-3-azabicyclo[3.2.1]-oct-8-yl)(methyl)amino]-1-(3,4-dimethoxyphenoxy)butyl]benzonitrile (see step (i) above; 2.20 g, 4.08 mmol) in diethyl ether (50 mL) at 0° C. Concentration in vacuo gave the HCl salt. The HCl salt and 10% palladium on carbon (220 mg) were suspended in methanol (20 mL) and stirred under an atmosphere of hydrogen overnight at 40° C. The catalyst was removed by filtration through a short pad of Celite®, washing with methanol (50 mL). The filtrate was concentrated in vacuo and chromatographed on silica gel, eluting with dichloromethane:methanol concentrated ammonium hydroxide (88:10:2), to afford 502 mg (28%) of the title compound as an off-white foam.

Mp: 47-53° C.; ¹H NMR (300 MHz, CD₃OD): δ 7.62 (d, J=8.2 Hz, 2H), 7.46 (d, J=8.2 Hz, 2H), 6.62 (d, J=8.2 Hz, 2H), 6.50 (s, 1H), 6.18 (d, J=4.0 Hz, 2H), 5.22-5.10 (m, 1H), 3.80 (s, 3H), 3.76 (s, 3H), 3.33-3.20 (m, 2H), 2.50-2.30 (m, 6H), 2.15 (s, 3H), 2.20-2.0 (m, 3H), 1.92-1.50 (m, 5H). ¹³C NMR (75 MHz, CD₃OD): δ 152.0, 149.8, 148.2, 143.6, 132.4, 128.0, 118.4, 112.0, 111.7, 105.6, 102.2, 79.6, 68.4, 57.6, 56.4, 55.8, 50.5, 44.6, 39.8, 35.8, 35.4, 26.2, 22.4. CI-MS: (M+1)=450 m/z.

Preparation K 4-{2-[8-(Methylamino)-3-azabicyclo[3.2.1]oct-3-yl]ethoxy}benzonitrile

(i) 4-(2-Bromoethoxy)benzonitrile

A mixture of 4-cyanophenol (35.7 g, 0.3 mol), K₂CO₃ (41.4 g, 0.3 mol) and 1,2-dibromoethane (561 g, 3.0 mol) in MeCN (450 mL) was stirred under reflux overnight. The mixture was filtered and evaporated to give 30.2 g (45%) of the sub-title compound, which was used without further purification.

(ii) tert-Butyl 3-[2-(4-Cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl-(methyl)carbamate

A mixture of 4-(2-bromoethoxy)benzonitrile (see step (i) above; 0.94 g, 4.2 mmol), tert-butyl 3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate (Preparation D; 0.91 g, 3.8 mmol) and K₂CO₃ (0.79 g, 5.7 mmol) in 15 mL of dry DMF was stirred at 90° C. overnight before additional K₂CO₃ (1 g) was added. The mixture was diluted with 300 mL of DCM, and the mixture was washed with water. The organic layer was separated, dried with Na₂SO₄ and then evaporated. The crude product was purified by flash chromatography on silica gel, eluting with DCM:MeOH (10:1) containing 0.1% TEA, to yield 1.1 g (76%) of the sub-tide compound.

(iii) 4-{2-[8-(Methylamino)-3-azabicyclo[3.2.1]oct-3-yl]ethoxy}-benzonitrile

Ethyl acetate (30 mL) saturated with gaseous HCl was added to a solution of tert-butyl 3-[2-(4-cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl-(methyl)carbamate (see step (ii) above; 1.1 g, 2.8 mmol) in ethyl acetate at 0° C. The resulting mixture was stirred for 4 h at rt. The solvent was removed in vacuo before MeCN (29 mL), water (1.5 mL) and K₂CO₃ (2.4 g) were added. The resulting mixture was stirred overnight before being filtered, washed with CHCl₃ and then concentrated in vacuo to give 0.79 g (99%) of the tide compound.

Preparation L 4-({3-[8-(Methylamino)-3-azabicyclo[3.2.1]oct-3-yl]propyl}sulfonyl)benzonitrile

(i) 4-[(3-Bromopropyl)sulfanyl]benzonitrile

A mixture of 4-cyanothiophenol (20.8 g, 154 mmol), 1,3-dibromopropane (155 g, 0.77 mol) and K₂CO₃ (21.3 g, 154 mmol) in MeCN (300 mL) was refluxed overnight. Filtration and evaporation of the solvent gave a brown oil that crystallised when treated with EtOH. The crystals were isolated by filtration to give the sub-title compound (24.5 g, 62%).

(ii) 4-[(3-Bromopropyl)sulfonyl]benzonitrile

3-Chloroperoxybenzoic acid (44.9 g of 70%, 182 mmol) was added slowly to a cooled (0° C.) solution of 4-[(3-bromopropyl)sulfanyl]-benzonitrile (see step (i) above; 23.4 g, 91 mmol) in DCM (250 mL). The mixture was then stirred at rt overnight, and the resulting precipitate filtered off. The filtrate was concentrated in vacuo to give a residue that was shown (by NMR analysis) to contain 25% sulfoxide in addition to the desired product. The residue was redissolved in DCM (250 mL), additional 3-chloroperoxybenzoic acid (5.6 g of 70%, 23 mmol) added, and the mixture stirred for 30 min. Dimethylsulfoxide (20 mmol) was added to destroy excess mCPBA before the DCM solution was washed with aqueous NaHCO₃, separated, dried and concentrated in vacuo. This gave the sub-title compound in 76% yield.

(iii) tert-Butyl 3-{3-[(4-cyanophenyl)sulfonyl]propyl}-3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate

The sub-title compound was obtained in 70% yield (1.1 g) according to the procedure described in Preparation K(ii) above, using 4-[(3-bromo-propyl)sulfonyl]benzonitrile (see step (ii) above) in place of 4-(2-bromoethoxy)benzonitrile.

(iv) 4-({3-[8-(Methylamino)-3-azabicyclo[3.2.1]oct-3-yl]propyl}sulfonyl)benzonitrile

The tide compound was obtained in 100% yield according to the procedure described in Preparation K (iii) above, using tert-butyl 3-{3-[(4-cyanophenyl)sulfonyl]propyl}-3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate (see step (iii) above) in place of tert-butyl 3-[2-(4-cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate.

Preparation M 4-{2-[8-(Methylamino)-3-azabicyclo[3.2.1]oct-3-yl]ethoxy}isophthalonitrile

(i) 4-(2-Bromoethoxy)isophthalonitrile

The sub-tide compound was prepared in 64% yield according to the procedure described in Preparation K(i) above, using 4-hydroxyisophthalonitrile in place of 4-cyanophenol.

(ii) tert-Butyl 3-[2-(2,4-Dicyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate

The sub-tide compound was prepared in 85% yield according to the procedure described in Preparation K(ii) above, using 4-(2-bromoethoxy)isophthalonitrile (see step (i) above) in place of 4-(2-bromoethoxy)benzonitrile.

(iii) 4-{2-[8-(Methylamino)-3-azabicyclo[3.2.1]oct-3-yl]ethoxy}isophthalonitrile

The title compound was prepared in 20% yield according to the method described in Preparation K(iii) above, using tert-butyl 3-[2-(2,4-dicyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate in place of tert-butyl 3-[2-(4-cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate.

Preparation N 4-{1-(4-Hydroxyphenoxy)-4-[8-(methylamino)-3-azabicyclo[3.2.1]oct-3-yl]butyl}benzonitrile

(i) 4-{1-[4-(Tetrahydro-2H-pyran-2-yloxy)phenoxy]-3-butenyl}benzonitrile

A cooled (0° C.) mixture of 4-(1-hydroxy-3-butenyl)benzonitrile (4.93 g, 28.5 mmol) and 4-(tetrahydro-2H-pyran-2-yloxy)phenol (8.3 g, 42.7 mmol) in dry THF (200 mL) was treated with tributylphosphine (8.85 mL, 42.7 mmol), followed by 1,1′-(azodicarbonyl)dipiperidine (10.77 g, 42.7 mmol). After addition was complete, the reaction mixture was stirred at 0° C. for 10 min, before being stirred at rt overnight. The precipitate of tributylphosphine oxide was removed by filtration and the filtrate was concentrated in vacuo to give 24.6 g of crude product. This was purified by chromatography on silica gel, eluting with IPA:EtOAc:heptane (5:5:90), to give 4.6 g (47%) of the subtitle compound.

(ii) 4-{4-Hydroxy-1-[4-(tetrahydro-2H-pyran-2-yloxy)phenoxy]butyl}benzonitrile

Borane-dimethylsulfide complex (3.5 mL of 2 M in ether, 7 mmol) was added dropwise to a cooled (5° C.) solution of 4-{1-[4-(tetrahydro-2H-pyran-2-yloxy)phenoxy]-3-butenyl}benzonitrile (see step (i) above; 4.6 g, 13 mmol) in dry THF over a period of 15 min. The resulting mixture was stirred at between 0 and 5° C. for 1.5 h. Stirring was then continued for a further 4 h at rt. Water (14 mL) and NaBO₃ (5 g) were added and the mixture stirred overnight. Ether was added and the resulting organic layer was separated, washed with water and brine, dried and then evaporated. The resulting residue was purified by chromatography on silica gel, eluting with IPA:EtOAc:heptane (5:20:70), to give 2.44 g (58%) of the sub-title compound.

(iii) 4-(4-Cyanophenyl)-4-[4-(tetrahydro-2H-pyran-2-yloxy)phenoxy]butyl Methanesulfonate

A solution of 4-{4-hydroxy-1-[4-(tetrahydro-2H-pyran-2-yloxy)phenoxy]butyl}benzonitrile (see step (ii) above; 2.37 g, 6.45 mmol) and TEA (1.35 mL, 9.68 mmol) in DCM (10 mL) was cooled to −5° C. Methanesulfonyl chloride (0.65 mL, 8.38 mmol) in DCM (5 mL) was added slowly. After addition was complete, the temperature was maintained below 5° C. for 1 h before DCM and water were added. The organic layer was washed with water, dried (Na₂SO₄) and then evaporated to yield 2.87 g (100%) of the sub-title compound. This was used in the next step without further purification.

(iv) tert-Butyl 3-{4-(4-Cyanophenyl)-4-[4-(tetrahydro-2H-pyran-2-yloxy)phenoxy]butyl}-3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate

The sub-title compound was prepared in 93.4% yield according to the procedure described in Preparation K(ii) above, using 4-(4-cyanophenyl)-4-[4-(tetrahydro-2H-pyran-2-yloxy)phenoxy]butyl methanesulfonate (see step (iii) above) and MeCN in place of 4-(2-bromoethoxy)benzonitrile and DMF, respectively.

(v) 4-{1-(4-Hydroxyphenoxy)-4-[8-(methylamino)-3-azabicyclo[3.2.1]oct-3-yl]butyl}benzonitrile

The title compound was prepared in 83.4% yield according to the method described in Preparation K(iii) above, using tert-butyl 3-{4-(4-cyanophenyl)-4-[4-(tetrahydro-2H-pyran-2-yloxy)phenoxy]butyl}-3-azabicyclo-[3.2.1]oct-8-yl(methyl)carbamate (see step (iv) above) in place of tert-butyl 3-[2-(4-cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate.

Preparation O Methyl (1S)-2-(4-Cyanophenoxy)-1-{[8-(methylamino)-3-azabicyclo[3.2.1]oct-3-yl]methyl}ethylcarbamate

(i) 4-[(2R)-Oxiranylmethoxy]benzonitrile

The title compound was prepared according to the procedure described in Preparation E(i) above, using S-epichlorohydrin in place of epichlorohydrin.

(ii) 4-{[(2R)-3-Amino-2-hydroxypropyl]oxy}benzonitrile

4-[(2R)-Oxiranylmethoxy]benzonitrile (see step (i) above; 14.65 g, 83.6 mmol) was mixed with NH₄OH (conc., 64 mL) and 87 mL of isopropanol. The mixture was stirred at rt for 18 h. The reaction mixture was then filtered and evaporated to give 14.6 g (91%) of the sub-title compound as a white solid.

(iii) Benzyl (2R)-3-(4-Cyanophenoxy)-2-hydroxypropylcarbamate

A mixture of 4{[(2R)-3-amino-2-hydroxypropyl]oxy}benzonitrile (see step (ii) above; 3.4 g, 17.7 mmol), TEA (2.69 g, 26.6 mmol) and CHCl₃ (20 mL) was cooled to 0° C. before N-(benzyloxycarbonyloxy)succinimide (4.86 g, 19.5 mol) in CHCl₃ (15 mL) was added slowly. The mixture was allowed to reach rt, and was stirred at that temperature overnight. The solvent was evaporated to give a residue that was dissolved in DCM. This solution was washed with water and brine and then dried (Na₂SO₄). Evaporation of the solvent gave 5.79 g (100%) of the sub-title compound.

(iv) (1R)-2-{[(Benzyloxy)carbonyl]amino}-1-[(4-cyanophenoxy)methyl]ethyl Methanesulfonate

4-(Dimethylamino)pyridine (0.22 g, 1.77 mmol) was added to a solution of benzyl (2R)-3-(4-cyanophenoxy)-2-hydroxypropylcarbamate (see step (iii) above; 5.79 g, 17.7 mmol) in pyridine (15 mL). The mixture was cooled to 0° C., and methanesulfonyl chloride (2.23 g, 19.5 mmol) was added slowly at 0° C. The mixture was allowed to reach rt, at which temperature it was then stirred for 4 h. The solvent was evaporated. DCM (100 mL) was added, washed with water, 1 N H₂SO₄ and brine, dried (Na₂SO₄) and evaporated giving 6.0 g (84%) of a yellow oil.

(v) Benzyl (2S)-2-[(4-Cyanophenoxy)methyl]-1-aziridinecarboxylate

A solution of NaOH in water (11 mL of 50 wt. %) was added under vigorous stirring to a solution of (1R)-2-{[(benzyloxy)carbonyl]amino}-1-[(4-cyanophenoxy)-methyl]ethyl methanesulfonate (see step (iv) above; 5.7 g, 14.1 mmol) and tetrabutylammonium hydrogensulfate (0.6 g, 1.7 mmol) in DCM (34 mL). The mixture was stirred for 1 h before water (200 mL) and ether (200 mL) were added. The organic phase was washed with water and then dried. The solvents were evaporated and the resulting residue was purified by chromatography (DCM eluant) to yield 3.0 g (69%) of the sub-title compound.

vi) Benzyl (1S)-2-{8-[(tert-Butoxycarbonyl)(methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}-1-[(4-cyanophenoxy)methyl]ethylcarbamate

Benzyl (2S)-2-[(4-cyanophenoxy)methyl]-1-aziridinecarboxylate (see step v) above; 1.3 g, 4.2 mmol) and tert-butyl 3-azabicyclo[3.2.1]oct-8-yl-methyl)carbamate (Preparation D; 1.1 g, 4.6 mmol) were mixed in IPA (15 mL) and stirred at 60° C. overnight. The solvent was then evaporated to give a residue that was purified by chromatography on silica gel, eluting with DCM:MeOH (100:3), to give 1.9 g (82%) of the sub-title compound.

(vii) tert-Butyl 3-[(2S)-2-Amino-3-(4-cyanophenoxy)propyl]-3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate

Benzyl (1S)-2-{8-[(tert-butoxycarbonyl)(methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}-1-[(4-cyanophenoxy)methyl]ethylcarbamate (see step (vi) above; 1.8 g, 3.3 mmol) was dissolved in ethanol (50 mL of 95%). The solution was hydrogenated over 5% Pd/C for 1 h, after which the mixture was filtered through Celite®. The filtrate was concentrated in vacuo to give 1.3 g (95%) of the sub-title compound.

(viii) Methyl (1S)-2-{8-[(tert-butoxycarbonyl)(methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}-1-[(4-cyanophenoxy)methyl]ethylcarbamate

Methyl chloroformate (0.24 mL, 3.2 mmol) was added, at 0° C., to a mixture of tert-butyl 3-[(2S)-2-amino-3-(4-cyanophenoxy)propyl]-3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate (see step (vii) above; 1.2 g, 2.9 mmol) and TEA (1.2 mL, 9 mmol) in DCM (30 mL). The mixture was allowed to reach rt over the course of 3 h, after which time a saturated solution of Na₂CO₃ was added. The organic phase was separated, dried and evaporated to give a crude product that was purified by chromatography on silica gel. This gave 0.6 g (45%) of the sub-title compound.

(ix) Methyl (1S)-2-(4-Cyanophenoxy)-1-{[8-(methylamino)-3-azabicyclo[3.2.1]oct-3-yl]methyl}ethylcarbamate

The title compound was prepared in 87% yield according to the procedure described in Preparation K(iii) above, using methyl (1S)-2-{8-[(tert-butoxycarbonyl)(methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}-1-[(4-cyanophenoxy)methyl]ethylcarbamate (see step (viii) above) in place of tert-butyl 3-[2-(4-cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate.

Preparation P tert-Butyl (1S)-2-(4-Cyanophenoxy)-1-{[8-(methylamino)-3-azabicyclo[3.2.1]oct-3-yl]methyl}ethylcarbamate

(i) tert-Butyl (2R)-3-(4-Cyanophenoxy)-2-hydroxypropylcarbamate

4-{[(2R)-3-amino-2-hydroxypropyl]oxy}benzonitrile (Preparation O(ii); 6.8 g, 3.5 mmol) was dissolved in a mixture of THF/water (8:1). The solution was cooled with an ice bath, and di-tert-butyl dicarbonate (7.7 g, 3.5 mmol) was added in portions. The mixture was stirred at rt overnight before the solvents were evaporated and DCM added. The resulting solution was washed with water, dried (Na₂SO₄) and evaporated to give 9.2 g of the sub-title compound.

(ii) (1R)-2-[(tert-Butoxycarbonyl)amino]-1-[(4-cyanophenoxy)methyl]ethyl Methanesulfonate

The sub-title compound was prepared in 100% yield according to the procedure described in Preparation O(iv) above, using tert-butyl (2R)-3-(4-cyanophenoxy)-2-hydroxypropylcarbamate (see step (i) above) in place of benzyl (2R)-3-(4-cyanophenoxy)-2-hydroxypropylcarbamate.

(iii) tert-Butyl (2S)-2-[(4-Cyanophenoxy)methyl]-1-aziridinecarboxylate

The sub-title compound was prepared according to the procedure described in Preparation O(v) above, using (1R)-2-[(tert-butoxycarbonyl)amino]-1-[(4-cyanophenoxy)methyl]ethyl methanesulfonate (see step (ii) above) in place of (1R)-2-{[(benzyloxy)carbonyl]amino}-1-[(4-cyanophenoxy)methyl]ethyl methanesulfonate.

(iv) tert-Butyl Methyl[3-(2,2,2-trifluoroacetyl)-3-azabicyclo[3.2.1]oct-8-yl]carbamate

Trifluoroacetic anhydride (10.5 g, 50 mmol) was added dropwise to a cooled (0° C.) mixture of tert-butyl 3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate (Preparation D; 11.1 g, 46 mmol), TEA (5.6 g, 55 mmol) and toluene (120 mL). The mixture was stirred for 3 h, and then evaporated. The resulting residue was dissolved in DCM and the resulting solution was washed with 1 M HCl (cold). The organic layer was separated, dried and evaporated to yield 14.8 g (96%) of the sub-title compound.

(v) 2,2,2-Trifluoro-1-[8-(methylamino)-3-azabicyclo[3.2.1]oct-3-yl]-1-ethanone

Ethyl acetate (100 mL) saturated with HCl (g) was added, at 0° C., to a solution of tert-butyl methyl[3-(2,2,2-trifluoroacetyl)-3-azabicyclo[3.2.1]oct-8-yl]carbamate (see step (iv) above; 5 g, 15 mmol) in ethyl acetate (50 mL). The mixture was allowed to reach rt over the course of 3 h, after which time the solvent was evaporated. This gave 4 g (100%) of the sub-tide compound hydrochloride salt.

(vi) 1-{8-[Benzyl(methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl]-2,2,2-trifluoro-1-ethanone

A mixture of 2,2,2-trifluoro-1-[8-(methylamino)-3-azabicyclo[3.2.1]oct-3-yl]-1-ethanone (see step (v) above; 4.5 g, 16 mmol), benzylchloride (3.0 g, 16 mmol) and TEA (6.6 mL) in MeCN (50 mL) was stirred at 60° C. overnight. The mixture was evaporated and then DCM and water were added. The organic phase was washed with NaHCO₃ solution, dried (Na₂SO₄) and then evaporated. The resulting crude product was purified by chromatography on silica gel (DCM eluant) to give 2.2 g (42%) of the sub-title compound.

(vii) N-Benzyl-N-methyl-3-azabicyclo[3.2.1]octan-8-amine

A mixture of 1-{8-[benzyl(methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}-2,2,2-trifluoro-1-ethanone (see step (vi) above; 2.1 g, 6.4 mmol) and K₂CO₃ (3 g, 21.7 mmol) in MeOH/water (110 mL of 10:1) was stirred at rt overnight and then evaporated. DCM and water were added and the layers separated. The water layer was extracted with DCM (3×). The combined organic layers were dried and evaporated to give 1.2 g (81%) of the sub-title compound.

(viii) tert-Butyl (1S)-2-{8-[Benzyl(methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}-1-[(4-cyanophenoxy)methyl]ethylcarbamate

A mixture of tert-butyl (2S)-2-[(4-cyanophenoxy)methyl]-1-aziridinecarboxylate (see step (iii) above; 1.26 g, 4.6 mmol) and N-benzyl-N-methyl-3-azabicyclo[3.2.1]octan-8-amine (see step (vii) above; 1.05 g, 4.6 mmol) in IPA (15 mL) was stirred at 60° C. overnight. The solvent was evaporated and the residue purified by chromatography on silica gel, eluting with DCM:MeOH (20:1). This gave 1.8 g (78%) of the subtitle compound

(ix) tert-Butyl (1S)-2-(4-Cyanophenoxy)-1-{[8-(methylamino)-3-azabicyclo[3.2.1]oct-3-yl]methyl}ethylcarbamate

A mixture of tert-butyl (1S)-2-{8-[benzyl(methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}-1-[(4-cyanophenoxy)methyl]ethylcarbamate (0.8 g, 1.6 mmol), 1 M HCl (0.8 mL) and MeOH (30 mL) was hydrogenated over 5% Pd/C. The reaction was stopped when the amount of H₂ calculated for complete reaction had been consumed. The mixture was filtered through silica and the filtrate evaporated. The resulting crude product was purified on silica gel, eluting with DCM:ammoniacal methanol (9:1), to yield 0.4 g (61%) of the title compound.

Preparation Q 2-(Acetyloxy)-1,1-dimethylethyl 1H-Imidazole-1-carboxylate

A mixture of 2-hydroxy-2-methylpropyl acetate (3.35 g, 25.3 mmol) and 1,1′-carbonyldiimidazole (4.11 g, 25.3 mmol) in DCM was stirred for 8 h at rt. The mixture was then transferred to a closed vessel and heated to 100° C. overnight. The mixture was concentrated in vacuo before ether and water were added. The organic phase was separated, dried and concentrated in vacuo. The resulting residue was purified by chromatography on silica gel, eluting with THF:heptane (1:1), to give the title compound in 20% yield.

Preparation R 1-Cyano-1-methylethyl 1H-Imidazole-1-carboxlate

A mixture of 1,1′-carbonyldiimidazole (5 g, 31 mmol) and 2-hydroxy-2-methylpropanenitrile (2.6 g, 31 mmol) in DCM was stirred at rt overnight. Water was added and the organic layer was separated, dried (Na₂SO₄) and concentrated in vacuo. The resulting residue was purified by chromatography on silica gel, eluting with ethyl acetate, to give 2.7 g (50%) of the title compound.

Preparation S 2-(4-Morpholinyl)ethyl 1H-Imidazole-1-carboxylate

A mixture of 1,1′-carbonyldiimidazole (6.5 g, 40 mmol) and 2-(4-morpholinyl)-1-ethanol (5.0 g, 38.1 mmol) in DCM (200 mL) was stirred for 22 h at rt. Ether (400 mL) was added and the mixture was washed with water. The water layer was then extracted with DCM. The combined organic layers were dried over Na₂SO₄ and evaporated to give 6.0 g (70%) of the tide compound.

Preparation T 2-(4-Pyridinyl)ethyl 1H-Imidazole-1-carboxylate

The title compound was prepared in 100% yield according to the procedure described in Preparation S above, using 2-(4-pyridinyl)-1-ethanol in place of 2-(4-morpholinyl)-1-ethanol.

Preparation U N-[2-(2-Methoxyethoxy)ethyl]-1H-imidazole-1-carboxamide

The title compound was prepared in 40% yield according to the procedure described in Preparation S above, using 2-(2-methoxyethoxy)ethylamine in place of 2-(4-morpholinyl)-1-ethanol.

Preparation V 2-(4-Acetyl-1-piperazinyl)ethyl 1H-Imidazole-1-carboxylate

(i) 1-[4-(2-Hydroxyethyl)-1-piperazinyl]-1-ethanone

A solution of 2-(1-piperazinyl)-1-ethanol (6.5 g, 0.05 mol) in DCM (5 mL) was treated with acetic acid anhydride (5.1 g, 0.05 mol), added dropwise. During addition, the reaction temperature rose from 22 to 60° C. The reaction mixture was evaporated several times with toluene to yield 5.6 g (65%) of the sub-title compound.

(ii) 2-(4-Acetyl-1-piperazinyl)ethyl 1H-Imidazole-1-carboxylate

A solution of 1,1′-carbonyldiimidazole (5 g, 31 mmol) in DCM (200 mL) was treated with a solution of 1-[4-(2-hydroxyethyl)-1-piperazinyl]-1-ethanone (see step (i) above; 5 g, 29 mmol) in DCM (50 mL). The reaction mixture was stirred at rt overnight before water was added. The layers were separated, and the organic layer was washed with water, dried and concentrated in vacuo to yield 7.4 g (96%) of the title compound.

Preparation W 1-[4-(3-Bromopropyl)-1-piperazinyl]-1-ethanone

A mixture of 1-(1-piperazinyl)-1-ethanone (6.7 g, 0.052 mol), dibromopropane (330 mL, excess) and K₂CO₃ (10.2 g, 0.079 mol) was stirred at rt for 4 h. The mixture was washed with 4×100 mL of water, and the organic phase (diluted with DCM) was acidified with aqueous hydrobromic acid (7 mL of 62% HBr dissolved in 150 mL of water). The organic layer was separated and washed with water (2×50 mL). The combined water layers were extracted with ether, neutralised (to pH 7) with 13 mL of 10 M NaOH, and then extracted with DCM. The combined organic layers were dried and concentrated in vacuo to give 4.1 g (32%) of the title compound.

Preparation X 3-(Ethylsulfonyl)propyl 4-Methylbenzenesulfonate

(i) 3-(Ethylsulfonyl)-1-propanol

A solution of 3-(ethylthio)-1-propanol (13 g, 0.11 mol) in acetic acid (40 mL) was treated with H₂O₂ (30% in water, 12.2 g, 0.11 mol), added dropwise. The mixture was stirred for 2 h at rt, before being concentrated in vacuo. NMR analysis showed that the resulting residue consisted of 40% of the desired product and 60% of the corresponding O-acetate. The acetate was hydrolysed by dissolving the reaction mixture in 200 mL of methanol and adding 3 g of NaOH (dissolved in a small amount of water). This mixture was stirred overnight at rt, then concentrated in vacuo. The resulting crude product was dissolved in DCM, and insoluble material was filtered off. The DCM was removed by evaporation to give 13.4 g (88%) of the sub-title compound.

(ii) 3-(Ethylsulfonyl)propyl 4-Methylbenzenesulfonate

A mixture of 3-(ethylsulfonyl)-1-propanol (see step (i) above; 13.4 g, 88 mmol) and p-toluenesulfonyl chloride (16.8 g, 88 mmol) in DCM (150 mL) was treated with TEA (13.4 g, 132 mmol), added dropwise. The resulting mixture was stirred at rt for 3 h before being washed with aqueous ammonium chloride solution. The organic layer was then separated, dried and concentrated in vacuo. The product was crystallised from ether containing a small amount of DCM to yield 17.9 g (66%) of the title compound.

The following intermediates were either commercially available or were prepared according to published methods:

3,4-dimethoxyphenethyl methanesulfonate;

hexyl isocyante;

ethyl isocyante;

butanoyl chloride;

1-butanesulfonyl chloride;

1-chloropinacoline;

4-isocyanato-3,5-dimethylisoxazole;

p-toluenesulfonyl isocyanate;

4-methoxyphenyl isocyanate;

2-isocyanatotetrahydro-2H-pyran;

isopropyl isocyanate;

3,4-difluorophenyl isocyanate;

butyl isocyanate;

1-(isocyanatomethyl)cyclopropane;

2-(acetylamino)-4-methyl-1,3-thiazole-5-sulfonyl chloride;

4-nitrobenzenesulfonyl chloride;

N-acetylsulfanilyl chloride;

isopropylsulfonyl chloride;

3,4-dimethoxybenzenesulfonyl chloride;

5-chloro-1,3-dimethylpyrazole4-sulfonyl chloride;

1,1-dioxo-2,5-dihydro-1-thiophene-3-sulfonyl chloride;

ethanesulfonyl chloride;

ethyl chloroformate;

2-butyn-1-chloroformate;

2-methoxyethyl chloroformate;

hydantoin-5-acetic acid;

2-{[2-(acetylamino)acetyl]amino}acetic acid;

methoxyacetic acid;

DL-glyceric acid;

pyrrole-2-carboxylic acid;

2-methylpropionic acid;

benzofurazan-5-carboxylic acid;

2-hydroxy-3-butynoic acid;

3-(tert-butyl)-1-methyl-1H-pyrazole-5-carboxylic acid;

(chloromethyl)cyclopropane;

2-bromo-1-(2,3-dihydro-1,4-benzodioxin-6-yl)-1-ethanone;

N-isopropyl chloroacetamide;

1-bromo-2-(2-methoxyethoxy)ethane;

4-fluorobenzyl bromide;

2-bromo-4′-methoxyacetophenone;

4-(trifluoromethylthio)phenyl isocyanate;

3-(methylsulfonyl)propyl-1-choroformate; and

3-methylbutyric acid.

Synthesis of Compounds of Formula I Example 1 tert-Butyl 8-{[3-(4-Cyanoanilino)propyl](methyl)amino}-3-azabicyclo[3.2.1]octane-3-carboxylate

A mixture of 4-({3-[3-azabicyclo[3.2.1]oct-8-yl(methyl)amino]propyl}amino)benzonitrile (Preparation H; 170 mg, 0.569 mmol) and di-tert-butyldicarbonate (124 mg, 0.569 mmol) in dichloromethane (3.0 mL) was stirred for 2 h at 25° C. under nitrogen. The mixture was concentrated in vacuo and the residue chromatographed on silica gel, eluting with ethyl acetate:dichloromethane (1:2), to yield 90 mg (40%) of the title compound as a colorless oil.

¹H NMR (300 MHz, CDCl₃): δ 7.40 (d, J=8.2 Hz, 2H), 6.50 (d, J=8.2 Hz, 2H), 5.45 (s, 1H), 3.68-3.60 (m, 1H), 3.52-3.40 (m, 1H), 3.32-3.10 (m, 4H), 2.60 (s, 2H), 2.30 (s, 3H), 2.22-2.15 (m, 3H), 1.92-1.60 (m, 6H), 1.45 (s, 9H). ¹³C NMR (75 MHz, CDCl₃): δ 156.4, 151.6, 133.6, 120.6, 112.0, 108.1, 79.4, 67.8, 54.2, 45.0, 44.0, 42.7, 39.8, 35.6, 28.4, 26.0, 25.4. CI-MS: (M+1)=399 m/z.

Example 2 tert-Butyl 8-[[3-(4-Cyanophenoxy)-2-hydroxypropyl](methyl)amino]-3-azabicyclo[3.2.1]octane-3-carboxylate

A mixture of 4-{3-[3-azabicyclo[3.2.1]oct-8-yl(methyl)amino]-2-hydroxypropoxy}benzonitrile (Preparation E; 229 mg, 0.726 mmol) and di-tert-butyldicarbonate (158 mg, 0.726 mmol) in dichloromethane (3.0 mL) was stirred for 2 h at 25° C. under nitrogen. The mixture was concentrated in vacuo and the residue chromatographed on silica gel, eluting with ethyl acetate:dichloromethane (1:2), to yield 70 mg (25%) of the tide compound as a colorless oil.

¹H NMR (300 MHz, CDCl₃): δ 7.58 (d, J=8.2 Hz, 2H), 6.97 (d, J=8.2 Hz, 2H), 4.30-4.16 (m, 1H), 4.12-4.0 (m, 2H), 3.70-3.10 (m, 5H), 2.82-2.70 (m, 1H), 2.52-2.10 (m, 4H), 2.30 (s, 3H), 1.80-1.52 (m, 4H), 1.45 (s, 9H). ¹³C NMR (75 MHz, CDCl₃): δ 162.4, 156.5, 134.0, 119.5, 115.6, 104.4, 79.5, 70.6, 68.0, 66.0, 57.7, 45.0, 43.8, 40.4, 36.8, 36.2, 28.5, 27.8. CI-MS: (M+1)=416 m/z.

Example 3 N-{3-[2-(4-Cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl}-N′-ethyl-N-methylurea

A solution of ethyl isocyanate (0.8 mL, 9.66 mmol) in DCM (3 mL) was added dropwise, at 0° C., to a mixture of 4-{2-[8-(methylamino)-3-azabicyclo[3.2.1]oct-3-yl]ethoxy}benzonitrile (Preparation K; 2.5 g, 8.76 mmol) and MeCN (50 mL). The mixture was stirred at rt for 3 h, K₂CO₃ (2 g, 14.4 mmol) was added and the mixture was stirred for a further 2 h. Filtration and evaporation gave 2.96 g of crude product. This was purified twice by chromatography on silica gel, the first time eluting with a gradient of EtOAc:MeOH:ammoniacal methanol (10:1:0 to 10:0:1), and the second time eluting with DCM:MeOH:TEA (190:10:1). This gave 2.3 g (71.4%) of the title compound.

¹³C NMR (CD₃OD): δ 15.84, 26.98, 36.35, 36.54, 38.70, 55.02, 57.88, 61.99, 67.68, 104.67, 116.66, 120.11, 135.16, 163.68, 163.94. MS(ES): (M+1)=357.0 m/z.

Example 4 N-{3-[3-(4-Cyanoanilino)propyl]-3-azabicyclo[3.2.1]oct-8-yl)-N-methyl-1-butanesulfonamide

A solution of 1-butanesulfonyl chloride (39.1 mg, 0.25 mmol) in MeCN (2 mL) was added to a solution of 4-({3-[8-(methylamino)-3-azabicyclo[3.2.1]oct-3-yl]propyl}amino)benzonitrile (Preparation G; 74.6 mg, 0.25 mmol) in CHCl₃ (0.5 mL). K₂CO₃ was added and the mixture was stirred at rt for 24 h. The mixture was filtered through a silica plug (500 mg), which plug was then eluted with MeCN:CHCl₃ (80:20; 3×2.5 mL), followed by CHCl₃:MeOH (95:5), to give the title compound in 35% yield.

MS(ES): (M+1)=419.2 m/z.

Example 5 Ethyl 3-[3-(4-Cyanoanilino)propyl]-3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate

A mixture of 4-({3-[8-(methylamino)-3-azabicyclo[3.2.1]oct-3-yl]propyl}amino)benzonitrile (Preparation G; 74.6 mg, 0.25 mmol) and ethyl chloroformate (29.8 mg, 0.27 mmol) in DMF (2.5 mL) was stirred at rt for 24 h. Mass spectroscopic analysis showed that the amine starting material had not been totally consumed, and so additional ethyl chloroformate (50 μL) was added. The mixture was stirred overnight, after which time it was concentrated in vacuo. The resulting residue was dissolved in a mixture of DCM (0.5 mL) and MeCN (2 mL). K₂CO₃ (100 mg, 0.7 mmol) was added and the mixture stirred for 4 h. Filtration of the mixture and evaporation of the filtrate gave a residue that was dissolved in CHCl₃ (1 mL). The solution was filtered through an ion-exchange solid-phase extraction plug (CBA, 2 g). The source flask was washed with additional CHCl₃ (0.75 mL), which was then added to the extraction plug, and eluted as fraction 1. The plug was then eluted with CHCl₃:MeOH:TEA (8:1:1; 4×2 mL) to give further fractions that were found not to contain any product. Fraction 1 was then added to a silica plug, which was eluted with CHCl₃:MeCN (4:1; 3×2.5 mL). Evaporation of the fractions collected gave 79.6 mg (85.9%) of the title compound.

MS(ES): (M+1)=371.5 m/z.

Example 6 N-{3-[3-(4-Cyanoanilino)propyl]-3-azabicyclo[3.2.1]oct-8-yl}-N,3-dimethylbutanamide

1,3-Dicyclohexylcarbodiimide on N-methylpolystyrene (0.67 g of 2.39 mmol/g, 1.74 mmol) was added to a solution of 4-({3-[8-(methylamino)-3-azabicyclo[3.2.1]oct-3-yl]propyl}amino)benzonitrile (Peparation G; 74.6 mg, 0.25 mmol) in DMF (3.0 mL). A solution of 3-methylbutyric acid (105.0 mg, 1.02 mmol) in DCM (1.0 mL) was added, and the mixture was stirred overnight at rt, followed by a further 72 h at 50° C. Polystyrene isocyanate (150 mg) and DCM (1.5 mL) were added, and this mixture was stirred for 1.5 h. K₂CO₃ (75 mg) was added and the mixture stirred for an additional 5 h. The solvents were evaporated and DCM (3 mL) was added to the resulting residue. This mixture was added to an ion-exchange solid-phase extraction plug (CBA). The plug was washed with DCM:MeCN (4:1; 10 mL). The product was then eluted with DCM:MeOH:TEA (90:5:5; 7.5 mL) to give 75 mg (70.9%) of the title compound.

MS(ES): 383.3 m/z.

Example 7

The following compounds were prepared, from appropriate intermediates (such as those described hereinbefore), according to or by analogy with methods described herein and/or by standard solid or solution phase combinatorial chemistry techniques (mass spectra of the compounds, where recorded, are in brackets: unless otherwise stated, the values refer to (M+1) ions measured by electrospray):

4-{3-[(3-butyryl-3-azabicyclo[3.2.1]oct-8-yl)(methyl)amino]-2-hydroxypropoxy}benzonitrile (m/z=386.2);

4-{3-[[3-(butylsulfonyl)-3-azabicyclo[3.2.1]oct-8-yl](methyl)amino]-2-hydroxypropoxy}benzonitrile (m/z=436.2);

4-{3-[[3-(3,3-dimethyl-2-oxobutyl)-3-azabicyclo[3.2.1]oct-8-yl](methyl)amino]-2-hydroxypropoxy}benzonitrile (m/z=414.3);

4-{3-[[3-(3,4-dimethoxyphenethyl)-3-azabicyclo[3.2.1]oct-8-yl](methyl)amino]-2-hydroxypropoxy}benzonitrile (m/z=480.3);

8-[[3-(4-cyanoanilino)propyl](methyl)amino]-N-hexyl-3-azabicyclo[3.2.1]octane-3-carboxamide (m/z=426.3);

8-[[3-(4-cyanoanilino)propyl](methyl)amino]-N-ethyl-3-azabicyclo[3.2.1]octane-3-carboxamide (m/z=370.3);

4-({3-[(3-butyryl-3-azabicyclo[3.2.1]oct-8-yl)(methyl)amino]propyl}amino)benzonitrile (m/z=369.3);

4-({3-[[3-(butylsulfonyl)-3-azabicyclo[3.2.1]oct-8-yl](methyl)amino]propyl}amino)benzonitrile (m/z=419.2);

4-({3-[[3-(3,3-dimethyl-2-oxobutyl)-3-azabicyclo[3.2.1]oct-8-yl](methyl)amino]propyl}amino)benzonitrile (m/z=397.3);

4-({3-[[3-(3,4-dimethoxyphenethyl)-3-azabicyclo[3.2.1]oct-8-yl](methyl)amino]propyl}amino)benzonitrile (m/z=463.3);

8-[[4-(4-cyanophenyl)-4-(3,4-dimethoxyphenoxy)butyl](methyl)amino]-N-hexyl-3-azabicyclo[3.2.1]octane-3-carboxamide (m/z=577.4);

8-[[4-(4-cyanophenyl)-4-(3,4-dimethoxyphenoxy)butyl](methyl)amino]-N-ethyl-3-azabicyclo[3.2.1]octane-3-carboxamide (m/z=521.3);

4-[4-[(3-butyryl-3-azabicyclo[3.2.1]oct-8-yl)(methyl)amino]-1-(3,4-dimethoxyphenoxy)butyl]benzonitrile (m/z=520.3);

4-[4-[[3-(butylsulfonyl)-3-azabicyclo[3.2.1]oct-8-yl](methyl)amino]-1-(3,4-dimethoxyphenoxy)butyl]benzonitrile (m/z=570.3);

4-{1-(3,4-dimethoxyphenoxy)-4-[[3-(3,3-dimethyl-2-oxobutyl)-3-azabicyclo[3.2.1]oct-8-yl](methyl)amino]butyl}benzonitrile (m/z=548.3);

4-[4-[[3-(3,4-dimethoxyphenethyl)-3-azabicyclo[3.2.1]oct-8-yl](methyl)amino]-1-(3,4-dimethoxyphenoxy)butyl]benzonitrile (m/z=614.4);

N-{3-[3-(4-cyanophenoxy)-2-hydroxypropyl]-3-azabicyclo[3.2.1]oct-8-yl}-N-hexyl-N-methylurea (m/z=443.3);

N-{3-[3-(4-cyanophenoxy)-2-hydroxypropyl]-3-azabicyclo[3.2.1]oct-8-yl}-N-ethyl-N-methylurea (m/z=387.2);

N-{3-[3-(4-cyanophenoxy)-2-hydroxypropyl]-3-azabicyclo[3.2.1]oct-8-yl}-N-methylbutanamide (m/z=386.2);

4-(3-{8-[(3,3-dimethyl-2-oxobutyl)(methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}-2-hydroxypropoxy)benzonitrile (m/z=414.3);

N-{3-[3-(4-cyanoanilino)propyl]-3-azabicyclo[3.2.1]oct-8-yl}-N′-hexyl-N-methylurea (m/z=426.3);

N-{3-[3-(4-cyanoanilino)propyl]-3-azabicyclo[3.2.1]oct-8-yl}-N′-ethyl-N-methylurea (m/z=370.3);

N-{3-[3-(4-cyanoanilino)propyl]-3-azabicyclo[3.2.1]oct-8-yl}-N-methyl-butanamide (m/z=369.3);

4-[(3-{8-[(3,3-dimethyl-2-oxobutyl)(methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}propyl)amino]benzonitrile (m/z=397.3);

4-[(3-{8-[(3,4-dimethoxyphenethyl)(methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}propyl)amino]benzonitrile (m/z=463.3);

N-{3-[4-(4-cyanophenyl)-4-(3,4-dimethoxyphenoxy)butyl]-3-azabicyclo[3.2.1]oct-8-yl}-N′-hexyl-N-methylurea (m/z=577.4);

N-{3-[4-(4-cyanophenyl)-4-(3,4-dimethoxyphenoxy)butyl]-3-azabicyclo[3.2.1]oct-8-yl}-N-ethyl-N-methylurea (m/z=521.3);

N-{3-[4-(4-cyanophenyl)-4-(3,4-dimethoxyphenoxy)butyl]-3-azabicyclo[3.2.1]oct-8-yl}-N-methylbutanamide (m/z=520.3);

N-{3-[4-(4-cyanophenyl)-4-(3,4-dimethoxyphenoxy)butyl]-3-azabicyclo[3.2.1]oct-8-yl}-N-methyl-1-butanesulfonamide (m/z=570.3);

4-(1-(3,4-dimethoxyphenoxy)-4-{8-[(3,3-dimethyl-2-oxobutyl)(methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}butyl)benzonitrile (m/z=548.3);

4-[4-{8-[(3,4-dimethoxyphenethyl)(methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}-1-(3,4-dimethoxyphenoxy)butyl]benzonitrile (m/z=614.4);

N-{3-[3-(4-cyanophenoxy)-2-hydroxypropyl]-3-azabicyclo[3.2.1]oct-8-yl}-N-methyl-N′-tetrahydro-2H-pyran-2-ylurea (m/z=443);

N-{3-[3-(4-cyanophenoxy)-2-hydroxypropyl]-3-azabicyclo[3.2.1]oct-8-yl}-N′-(cyclopropylmethyl)-N-methylurea (m/z=413);

3-[3-(4-cyanoanilino)propyl]-8-[methyl({[(4-methylphenyl)sulfonyl]-amino}carbonyl)amino]-3-azabicyclo[3.2.1]octane (ES (M-1): m/z=494);

N-{3-[3-(4-cyanoanilino)propyl]-3-azabicyclo[3.2.1]oct-8-yl}-N′-(cyclo-propylmethyl)-N-methylurea (m/z=397);

N-{3-[3-(4-cyanoanilino)propyl]-3-azabicyclo[3.2.1]oct-8-yl}-N′-isopropyl-N-methylurea (m/z=384);

N′-butyl-N-{3-[3-(4-cyanoanilino)propyl]-3-azabicyclo[3.2.1]oct-8-yl}-N-methylurea (ES (M-1): m/z=396);

4-(3-{8-[(3,4-dimethoxyphenethyl)(methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}-2-hydroxypropoxy)benzonitrile (m/z=480.3);

3-[3-(4-cyanophenoxy)-2-hydroxypropyl]-8-[methyl({[(4-methylphenyl)sulfonyl]amino}carbonyl)amino]-3-azabicyclo[3.2.1]octane (ES (M-1): m/z=511);

N-{3-[3-(4-cyanophenoxy)-2-hydroxypropyl]-3-azabicyclo[3.2.1]oct-8-yl}-N′-(3,4-difluorophenyl)-N-methylurea (m/z=471);

N-{3-[3-(4-cyanoanilino)propyl]-3-azabicyclo[3.2.1]oct-8-yl}-N′-(4-methoxyphenyl)-N-methylurea (m/z=448);

N-{3-[3-(4-cyanoanilino)propyl]-3-azabicyclo[3.2.1]oct-8-yl}-N′-(3,4-difluorophenyl)-N-methylurea (m/z=454);

N-{3-[2-(4-cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl}-N′-(3,5-dimethyl-4-isoxazolyl)-N-methylurea (m/z=424);

N-{3-[2-(4-cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl}-N′-(4-methoxyphenyl)-N-methylurea (m/z=435);

N-{3-[2-(4-cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl}-N-methyl-N′-tetrahydro-2H-pyran-2-ylurea (m/z=413);

N-{3-[2-(4-cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl}-N′-(cyclopropylmethyl)-N-methylurea (m/z=383);

N-{3-[2-(4-cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl}-N′-isopropyl-N-methylurea (m/z=371);

N-{3-[2-(4-cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl}-N′-(3,4-difluorophenyl)-N-methylurea (m/z=441);

N-(3-{3-[(4-cyanophenyl)sulfonyl]propyl}-3-azabicyclo[3.2.1]oct-8-yl)-N′-(3,5-dimethyl-4-isoxazolyl)-N-methylurea (m/z=486);

3-{3-[(4-cyanophenyl)sulfonyl]propyl}-8-[methyl({[(4-methylphenyl)sulfonyl]amino}carbonyl)amino]-3-azabicyclo[3.2.1]octane (ES (M-1): m/z=543);

N-(3-{3-[(4-cyanophenyl)sulfonyl]propyl}-3-azabicyclo[3.2.1]oct-8-yl)-N′-(4-methoxyphenyl)-N-methylurea (m/z=497);

N-(3-{3-[(4-cyanophenyl)sulfonyl]propyl}-3-azabicyclo[3.2.1]oct-8-yl)-N′-(cyclopropylmethyl)-N-methylurea (m/z=445);

N-(3-{3-[(4-cyanophenyl)sulfonyl]propyl}-3-azabicyclo[3.2.1]oct-8-yl)-N′-(3,4-difluorophenyl)-N-methylurea (m/z=503);

N-(3-[3-(4-cyanophenoxy)-2-hydroxypropyl]-3-azabicyclo[3.2.1]oct-8-yl}-N-methyl-1-butanesulfonamide (m/z=436.2);

N-{3-[3-(4-cyanophenoxy)-2-hydroxypropyl]-3-azabicyclo[3.2.1]oct-8-yl}-3,4-dimethoxy-N-methylbenzenesulfonamide (m/z=516.2);

5-chloro-N-{3-[3-(4-cyanophenoxy)-2-hydroxypropyl]-3-azabicyclo[3.2.1]oct-8-yl}-N,1,3-trimethyl-1H-pyrazole4-sulfonamide (m/z=508.2);

N-(5-{[{3-[3-(4-cyanoanilino)propyl]-3-azabicyclo[3.2.1]oct-8-yl}(methyl)-amino]sulfonyl}-4-methyl-1,3-thiazol-2-yl)acetamnide (m/z=517.2);

N-{3-[3-(4-cyanoanilino)propyl]-3-azabicyclo[3.2.1]oct-8-yl}-N-methyl-4-nitrobenzenesulfonamide (m/z=484.2);

N-(4-{[{3-[3-(4-cyanoanilino)propyl]-3-azabicyclo[3.2.1]oct-8-yl}(methyl)amino]sulfonyl}phenyl)acetamide (m/z=496.2);

N-{3-[3-(4-cyanoanilino)propyl]-3-azabicyclo[3.2.1]oct-8-yl}-3,4-dimethoxy-N-methylbenzenesulfonamide (m/z=499.2);

5-chloro-N-{3-[3-(4-cyanoanilino)propyl]-3-azabicyclo[3.2.1]oct-8-yl}-N,1,3-trimethyl-1H-pyrazole-4-sulfonamide (m/z=491.2);

N-{3-[3-(4-cyanoanilino)propyl]-3-azabicyclo[3.2.1]oct-8-yl}-N-methyl-1-ethanesulfonamide (m/z=391.2);

N-(3-{3-[(4-cyanophenyl)sulfonyl]propyl}-3-azabicyclo[3.2.1]oct-8-yl)-N-methyl-4-nitrobenzenesulfonamide (m/z=533.1);

N-(3-{3-[(4-cyanophenyl)sulfonyl]propyl}-3-azabicyclo[3.2.1]oct-8-yl)-3,4-dimethoxy-N-methylbenzenesulfonamide (m/z=548.2);

N-(5-{[{3-[2-(4-cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl}-(methyl)amino]sulfonyl}4-methyl-1,3-thiazol-2-yl)acetamide (m/z=504.2);

N-{3-[2-(4-cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl}-N-methyl-4-nitrobenzenesulfonamide (m/z=471.2);

N-(4-([{3-[2-(4-cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl}-(methyl)amino]sulfonyl}phenyl)acetamnide (m/z=483.2);

N-{3-[2-(4-cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl)-N-methyl-2-propanesulfonamide;

N-{3-[2-(4-cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl}-3,4-dimethoxy-N-methylbenzenesulfonamide (m/z=486.2);

5-chloro-N-{3-[2-(4-cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl}-N,1,3-trimethyl-1H-pyrazole-4-sulfonamide (m/z=478.2);

N-{3-[2-(4-cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl}-N,1-dimethyl-1H-imidazole-4-sulfonamide (m/z=430.2);

2-butynyl 3-[3-(4-cyanophenoxy)-2-hydroxypropyl]-3-azabicyclo[3.2.1]-oct-8-yl(methyl)carbamate (m/z=412.5);

2-methoxyethyl 3-[3-(4-cyanophenoxy)-2-hydroxypropyl]-3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate (m/z=418.5);

3-(methylsulfonyl)propyl 3-[3-(4-cyanophenoxy)-2-hydroxypropyl]-3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate (m/z=480.5);

2-(4-acetyl-1-piperazinyl)ethyl 3-[3-(4-cyanophenoxy)-2-hydroxypropyl]-3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate;

2-hydroxy-1,1-dimethylethyl 3-[3-(4-cyanoanilino)propyl]-3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate;

1-cyano-1-methylethyl 3-[3-(4-cyanoanilino)propyl]-3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate (m/z=410.5);

2-butynyl 3-[3-(4-cyanoanilino)propyl]-3-azabicyclo[3.2.1]oct-8-yl-(methyl)carbamate (m/z=395.5);

2-methoxyethyl 3-[3-(4-cyanoanilino)propyl]-3-azabicyclo[3.2.1]oct-8-yl-(methyl)carbamate (m/z=401.6);

3-(methylsulfonyl)propyl 3-[3-(4-cyanoanilino)propyl]-3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate (m/z=463.5);

2-(4-pyridinyl)ethyl 3-[3-(4-cyanoanilino)propyl]-3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate (m/z=448.6);

N-{3-[3-(4-cyanoanilino)propyl]-3-azabicyclo[3.2.1]oct-8-yl}-N′-[2-(2-methoxyethoxy)ethyl]-N-methylurea (m/z=444.6);

ethyl 3-{3-[(4-cyanophenyl)sulfonyl]propyl}-3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate (m/z=420.5);

2-hydroxy-1,1-dimethylethyl 3-{3-[(4-cyanophenyl)sulfonyl]propyl}-3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate;

2-(4-morpholinyl)ethyl 3-{3-[(4-cyanophenyl)sulfonyl]propyl}-3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate (m/z=505.5);

N-(3-{3-[(4-cyanophenyl)sulfonyl]propyl}-3-azabicyclo[3.2.1]oct-8-yl)-N′-[2-(2-methoxyethoxy)ethyl]-N-methylurea (m/z=493.5);

ethyl 3-[2-(4-cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate (m/z=358.5);

2-hydroxy-1,1-dimethylethyl 3-[2-(4-cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate;

1-cyano-1-methylethyl 3-[2-(4-cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]-oct-8-yl(methyl)carbamate (m/z=397.5);

2-butynyl 3-[2-(4-cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl-(methyl)carbamate (m/z=382.5);

2-methoxyethyl 3-[2-(4-cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl-(methyl)carbamate (m/z=388.5);

3-(methylsulfonyl)propyl 3-[2-(4-cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate (m/z=450.5);

2-(4-pyridinyl)ethyl 3-[2-(4-cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl(methyl)carbamate (m/z=435.5);

N-{3-[3-(4-cyanophenoxy)-2-hydroxypropyl]-3-azabicyclo[3.2.1]oct-8-yl}-2-methoxy-N-methylacetamide (m/z=388.2);

N-{3-[3-(4-cyanophenoxy)-2-hydroxypropyl]-3-azabicyclo[3.2.1]oct-8-yl}-N,2-dimethylpropanamide (m/z=386.3);

N-{3-[3-(4-cyanophenoxy)-2-hydroxypropyl]-3-azabicyclo[3.2.1]oct-8-yl}-N,3-dimethylbutanamide (m/z=400.3);

N-{3-[3-(4-cyanophenoxy)-2-hydroxypropyl]-3-azabicyclo[3.2.1]oct-8-yl}-N-methyl-2,1,3-benzoxadiazole-5-carboxamide (m/z=461.5);

3-(tert-butyl)-N-{3-[3-(4-cyanophenoxy)-2-hydroxypropyl]-3-azabicyclo[3.2.1]oct-8-yl}-N,1-dimethyl-1H-pyrazole-5-carboxamide (m/z=480.3);

N-{3-[3-(4-cyanoanilino)propyl]-3-azabicyclo[3.2.1]oct-8-yl}-2-(2,5-dioxo-4-imidazolidinyl)-N-methylacetamide (m/z=439.3);

N-{3-[3-(4-cyanoanilino)propyl]-3-azabicyclo[3.2.1]oct-8-yl}-N-methyl-1H-pyrrole-2-carboxamide (m/z=392.3);

N-{3-[3-(4-cyanoanilino)propyl]-3-azabicyclo[3.2.1]oct-8-yl}-N,2-dimethylpropanamide (m/z=369.3);

N-{3-[3-(4-cyanoanilino)propyl]-3-azabicyclo[3.2.1]oct-8-yl}-N-methyl-2,1,3-benzoxadiazole-5-carboxamide (m/z=445.2);

3-(tert-butyl)-N-{3-[3-(4-cyanoanilino)propyl]-3-azabicyclo[3.2.1]oct-8-yl}-N,1-dimethyl-1H-pyrazole-5-carboxamide (m/z=463.3);

N-(3-{3-[(4-cyanophenyl)sulfonyl]propyl}-3-azabicyclo[3.2.1]oct-8-yl)-2-(2,5-dioxo-4-imidazolidinyl)-N-methylacetamide (m/z=488.2);

2-(acetylamino)-N-{2-[(3-{3-[(4-cyanophenyl)sulfonyl]propyl}-3-azabicyclo[3.2.1]oct-8-yl)(methyl)amino]-2-oxoethyl}acetamide (m/z=25 504.2);

N-(3-{3-[(4-cyanophenyl)sulfonyl]propyl}-3-azabicyclo[3.2.1]oct-8-yl)-N-methyl-2,1,3-benzoxadiazole-5-carboxamide (m/z=494.1);

N-{3-[2-(4-cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl}-2-(2,5-dioxo-4-imidazolidinyl)-N-methylacetamide (m/z=426.2);

N-{3-[2-(4-cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl}-N,2-dimethylpropanamide (m/z=356.2);

N-{3-[2-(4-cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl}-N,3-dimethylbutanamide (m/z=370.3);

N-{3-[2-(4-cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl}-N-methyl-2,1,3-benzoxadiazole-5-carboxamide (m/z=432.2);

3-(tert-butyl)-N-{3-[2-(4-cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl}-N,1-dimethyl-1H-pyrazole-5-carboxamide (m/z=450.3);

4-(3-{8-[(cyclopropylmethyl)(methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}-2-hydroxypropoxy)benzonitrile (m/z=370.5);

4-(3-{8-[[2-(2,3-dihydro-1,4-benzodioxin-6-yl)-2-oxoethyl](methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}-2-hydroxypropoxy)benzonitrile (m/z=492.5);

4-(3-{8-[[3-(4-acetyl-1-piperazinyl)propyl](methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}-2-hydroxypropoxy)benzonitrile (m/z=484.5);

2-[{3-[3-(4-cyanophenoxy)-2-hydroxypropyl]-3-azabicyclo[3.2.1]oct-8-yl}(methyl)amino]-N-isopropylacetamide (m/z 415.5);

4-(3-{8-[[3-(ethylsulfonyl)propyl](methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}-2-hydroxypropoxy)benzonitrile (m/z=450.5);

4-(3-{8-[(4-fluorobenzyl)(methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}-2-bydroxypropoxy)benzonitrile (m/z=424.5);

4-(2-hydroxy-3-{8-[[2-(4-methoxyphenyl)-2-oxoethyl](methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}propoxy)benzonitrile (m/z=464.5);

4-[(3-{8-[(cyclopropylmethyl)(methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}propyl)amino]benzonitrile (m/z=353.5);

4-[(3-{8-[[2-(2,3-dihydro-1,4-benzodioxin-6-yl)-2-oxoethyl](methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}propyl)amino]benzonitrile (m/z=475.5);

4-[(3-{8-[[3-(4-acetyl-1-piperazinyl)propyl](methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}propyl)amino]benzonitrile (m/z=467.6);

2-[{3-[3-(4-cyanoanilino)propyl]-3-azabicyclo[3.2.1]oct-8-yl}(methyl)amino]-N-isopropylacetamide (m/z=398.5);

4-[(3-{8-[[3-(ethylsulfonyl)propyl](methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}propyl)amino]benzonitrile (m/z=433.5);

4-[(3-{8-[(4-fluorobenzyl)(methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}-propyl)amino]benzonitrile (m/z=407.5);

4-[(3-{8-[[2-(4-methoxyphenyl)-2-oxoethyl](methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}propyl)amino]benzonitrile (m/z=447.5);

4-[(3-{8-[(3,3-dimethyl-2-oxobutyl)(methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}propyl)sulfonyl]benzonitrile (m/z=446.5);

4-[(3-{8-[(cyclopropylmethyl)(methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}-propyl)sulfonyl]benzonitrile (m/z=402.5);

4-[(3-{8-[[2-(2,3-dihydro-1,4-benzodioxin-6-yl)-2-oxoethyl](methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}propyl)sulfonyl]benzonitrile (m/z=524.4);

2-[(3-{3-[(4-cyanophenyl)sulfonyl]propyl}-3-azabicyclo[3.2.1]oct-8-yl)-(methyl)amino]-N-isopropylacetamide (m/z=447.5);

4-[(3-{8-[[3-(ethylsulfonyl)propyl](methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}propyl)sulfonyl]benzonitrile (m/z=482.4);

4-[(3-{8-[[2-(2-methoxyethoxy)ethyl](methyl)amino]-3-azabicyclo[3.2.1]-oct-3-yl}propyl)sulfonyl]benzonitrile (m/z=450.5);

4-[(3-{8-[(4-fluorobenzyl)(methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}-propyl)sulfonyl]benzonitrile (m/z=456.5);

4-[(3-{8-[[2-(4-methoxyphenyl)-2-oxoethyl](methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}propyl)sulfonyl]benzonitrile (m/z=496.4);

4-(2-{8-[(3,3-dimethyl-2-oxobutyl)(methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}ethoxy)benzonitrile (m/z=384.5);

4-(2-{8-[(cyclopropylmethyl)(methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}-ethoxy)benzonitrile (m/z=340.5);

4-(2-{8-[[2-(2,3-dihydro-1,4-benzodioxin-6-yl)-2-oxoethyl](methyl)-amino]-3-azabicyclo[3.2.1]oct-3-yl}ethoxy)benzonitrile (m/z=462.5);

2-[{3-[2-(4-cyanophenoxy)ethyl]-3-azabicyclo[3.2.1]oct-8-yl}(methyl)-amino]-N-isopropylacetamide (m/z=385.5);

4-(2-{8-[[2-(2-methoxyethoxy)ethyl](methyl)amino]-3-azabicyclo[3.2.1]-oct-3-yl}ethoxy)benzonitrile (m/z=388.5);

4-(2-{8-[(4-fluorobenzyl)(methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}-ethoxy)benzonitrile (m/z=394.5);

methyl (1S)-2-(4-cyanophenoxy)-1-({8-[methyl({[(4-methylphenyl)sulfonyl]amino}carbonyl)amino]-3-azabicyclo[3.2.1]oct 3-yl}methyl)ethylcarbamate (m/z=570.4);

methyl (1S)-2-(4-cyanophenoxy)-1-({8-[methyl({4-[(trifluoromethyl)sulfanyl]anilino}carbonyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}methyl)ethylcarbamate (m/z=592.3);

methyl (1S)-2-(4-cyanophenoxy)-1-[(8-{methyl[(tetrahydro-2H-pyran-2-ylamino)carbonyl]amino}-3-azabicyclo[3.2.1]oct-3-yl)methyl]-ethylcarbamate (m/z=500.5);

methyl (1S)-2-(4-cyanophenoxy)-1-({8-[{[(cyclopropylmethyl)amino]-carbonyl}(methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}methyl)ethylcarbamate (m/z=470.5);

methyl (1S)-2-(4-cyanophenoxy)-1-({8-[[(isopropylamino)carbonyl]-(methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}methyl)ethylcarbamate (m/z=458.5);

methyl (1S)-2-(4-cyanophenoxy)-1-({8-[[(3,4-difluoroanilino)carbonyl]-(methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}methyl)ethylcarbamate (m/z=528.5);

methyl (1S)-2-{8-[[(butylamino)carbonyl](methyl)amino]-3-azabicyclo[3.2.1]oct-3-yl}-1-[(4-cyanophenoxy)methyl]ethylcarbamate (m/z=472.5);

N-{3-[(2S)-2-amino-3-(4-cyanophenoxy)propyl]-3-azabicyclo[3.2.1]oct-8-s yl}-N′-(4-methoxyphenyl)-N-methylurea (m/z=464.5);

N-{3-[(2S)-2-amino-3-(4-cyanophenoxy)propyl]-3-azabicyclo[3.2.1]oct-8-yl}-N′-(cyclopropylmethyl)-N-methylurea (m/z=412.5);

N-{3-[(2S)-2-amino-3-(4-cyanophenoxy)propyl]-3-azabicyclo[3.2.1]oct-8-yl}-N′-(3,4-difluorophenyl)-N-methylurea (m/z=470.5);

N-{3-[(2S)-2-amino-3-(4-cyanophenoxy)propyl]-3-azabicyclo[3.2.1]oct-8-yl}-N′-butyl-N-methylurea (m/z=414.6);

N-{3-[4-(4-cyanophenyl)-4-(4-hydroxyphenoxy)butyl]-3-azabicyclo[3.2.1]-oct-8-yl}-N′-(3,5-dimethyl-4-isoxazolyl)-N-methylurea (m/z=544.5);

N-3-[4-(4-cyanophenyl)-4-(4-hydroxyphenoxy)butyl]-3-azabicyclo[3.2.1]-oct-8-yl}-N′-(4-methoxyphenyl)-N-methylurea (m/z=555.5);

N-3-[4-(4-cyanophenyl)-4-(4-hydroxyphenoxy)butyl]-3-azabicyclo[3.2.1]-oct-8-yl}-N-methyl-N′-{4-[(trifluoromethyl)sulfanyl]phenyl}urea (m/z=625.3);

N′-butyl-N-{3-[4-(4-cyanophenyl)-4-(4-hydroxyphenoxy)butyl]-3-azabicyclo[3.2.1]oct-8-yl}-N-methylurea (m/z=505.6); and

tert-butyl 3-[(2S)-2-amino-3-(4-cyanophenoxy)propyl]-3-azabicyclo[3.2.1]-oct-8-yl(methyl)carbamate (m/z=415.5).

Example 8

Compounds of the above Examples were tested in Test A above and were found to exhibit pIC50 values of greater than 5.5.

Abbreviations Ac = acetyl API = atmospheric pressure ionisation (in relation to MS) aq. = aqueous br = broad (in relation to NMR) Bt = benzotriazole t-BuOH = tert-butanol CI = chemical ionisation (in relation to MS) mCPBA = meta-chloroperoxybenzoic acid d = doublet (in relation to NMR) DBU = diazabicyclo[5.4.0]undec-7-ene DCM = dichloromethane dd = doublet of doublets (in relation to NMR) DMAP = 4-dimethylaminopyridine DMF = N,N-dimethylformamide DMSO = dimethylsulfoxide EDC = 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide Et = ethyl EtOAc = ethyl acetate eq. = equivalents ES = electrospray (in relation to MS) FAB = fast atom bombardment (in relation to MS) h = hour(s) HCl = hydrochloric acid HEPES = 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid HPLC = high performance liquid chromatography IPA = iso-propyl alcohol (propan-2-ol) m = multiplet (in relation to NMR) Me = methyl MeCN = acetonitrile MeOH = methanol min. = minute(s) m.p. = melting point MS = mass spectroscopy NADPH = nicotinamide adenine dinucleotide phosphate, reduced form OAc = acetate Pd/C = palladium on carbon q = quartet (in relation to NMR) rt = room temperature s = singlet (in relation to NMR) t = triplet (in relation to NMR) TEA = triethylamine THF = tetrahydrofuran tlc = thin layer chromatography Prefixes n-, s-, i-, t- and tert- have their usual meanings: normal, secondary, iso, and tertiary. 

What is claimed is:
 1. A compound of formula I,

wherein the wavy bond represents optional endo- or exo-stereochemistry; one of R¹ and R² represents R^(1a) and the other represents a fragment of the formula Ia,

R^(1a) represents C₁₋₁₂ alkyl (optionally substituted and/or terminated by one or more groups selected from halo, cyano, nitro, aryl, Het¹, —C(O)R^(7a), —OR^(7b), —N(R⁸)R^(7c), —C(O)XR⁹, —C(O)N(R¹⁰)R^(7d) and —S(O)₂R¹¹), Het², —C(O)R^(7a), —C(O)XR⁹, —C(O)N(R¹⁰)R^(7d) or —S(O)₂R¹¹; R^(7a) to R^(7d) independently represent, at each occurrence when used herein, H, C₁₋₆ alkyl (optionally substituted and/or terminated by one or more substituents selected from —OH, C₁₋₆ alkoxy, halo, cyano, nitro, aryl, Het³ and —NHC(O)R¹²), aryl or Het⁴, or R^(7d), together with R¹⁰, represents C₃₋₆ alkylene (which alkylene group is optionally interrupted by an O atom and/or is optionally substituted by one or more C₁₋₃ alkyl groups); R¹² represents H, C₁₋₄ alkyl (optionally substituted and/or terminated by one or more substituents selected from halo, cyano, aryl and —NHC(O)R¹³) or aryl; R¹³ represents H, C₁₋₄ alkyl or aryl; R⁸ represents H, C₁₋₆ alkyl (optionally substituted and/or terminated by one or more substituents selected from —OH, halo, cyano, nitro and aryl), aryl, —C(O)R^(14a) or —C(O)OR^(14b); R^(14a) and R^(14b) represent C₁₋₆ alkyl (optionally substituted and/or terminated by one or more substituents selected from —OH, halo, cyano, nitro and aryl) or aryl, or R^(14a) represents H; X represents O or S; R⁹ represents, at each occurrence when used herein, C₁₋₁₂ alkyl (optionally substituted and/or terminated by one or more substituents selected from —OH, halo, cyano, nitro, aryl, C₁₋₆ alkoxy, —SO₂R¹⁵ and Het⁵); R¹⁵ represents C₁₋₆ alkyl or aryl; R¹⁰ represents, at each occurrence when used herein, H, C₁₋₁₂ alkyl, C₁₋₆ alkoxy (which latter two groups are optionally substituted and/or terminated by one or more substituents selected from —OH, halo, cyano, nitro, C₁₋₄ alkyl and C₁₋₄ alkoxy), —D-aryl, —D-aryloxy, —D-Het⁶, —D—N(H)C(O)R^(16a), —D—S(O)₂R^(17a), —D—C(O)R^(16b), —D—C(O)OR^(17b), —D—C(O)N(R^(16c))R^(16d), or R¹⁰, together with R^(7d), represents C₃₋₆ alkylene (which alkylene group is optionally interrupted by an O atom and/or is optionally substituted by one or more C₁₋₃ alkyl groups); R^(16a) to R^(16d) independently represent H, C₁₋₆ alkyl (optionally substituted and/or terminated by one or more substituents selected from —OH, halo, cyano, nitro and aryl), aryl, or R^(16c) and R^(16d) together represent C₃₋₆, alkylene; R^(17a) and R^(17b) independently represent C₁₋₆ alkyl (optionally substituted and/or terminated by one or more substituents selected from —OH, halo, cyano, nitro and aryl) or aryl; D represents a direct bond or C₁₋₆ alkylene; R¹¹ represents, at each occurrence when used herein, C₁₋₆ alkyl (optionally substituted and/or terminated by one or more substituents selected from is —OH, halo, cyano, nitro and aryl), aryl or Het⁷; R⁴ represents H, halo, C₁₋₆ alkyl, —OR¹⁸, —E—N(R¹⁹)R²⁰ or, together with R⁵, represents ═O; R⁵ represents H, C₁₋₆ alkyl or, together with R⁴, represents ═O; R¹⁸ represents H, C₁₋₆ alkyl, —E-aryl, —E—Het⁸, —C(O)R^(21a), —C(O)OR^(21b) or —C(O)N(R^(22a))R^(22b); R¹⁹ represents H, C₁₋₆ alkyl, —E-aryl, —E—Het⁸, —C(O)R^(21a), —C(O)OR^(21b), —S(O)₂R^(21c), —[C(O)]_(p)N(R^(22a))R^(22b) or —C(NH)NH₂; R²⁰ represents H, C₁₋₆ alkyl, —E-aryl or —C(O)R^(21d); R^(21a) to R^(21d) independently represent, at each occurrence when used herein, C₁₋₆ alkyl (optionally substituted and/or terminated by one or more substituents selected from halo, aryl and Het⁹), aryl, Het¹⁰, or R^(21a) and R^(21d) independently represent H; R^(22a) and R^(22b) independently represent, at each occurrence when used herein, H or C₁₋₆ alkyl (optionally substituted and/or terminated by one or more substituents selected from halo, aryl and Het¹¹), aryl, Het¹², or together represent C₃₋₆ alkylene, optionally interrupted by an O atom; E represents, at each occurrence when used herein, a direct bond or C₁₋₄ alkylene; p represents 1 or 2; Het¹ to Het¹² independently represent, at each occurrence when used herein, five- to twelve-membered heterocyclic groups containing one or more heteroatoms selected from oxygen, nitrogen and/or sulfur, which groups are optionally substituted by one or more substituents selected from —OH, oxo, halo, cyano, nitro, C₁₋₆ alkyl, C₁₋₆ alkoxy, aryl, aryloxy, —N(R^(23a))R^(23b), —C(O)R^(23c), —C(O)OR^(23d), —C(O)N(R^(23e))R^(23f), —N(R^(23g))C(O)R^(23h) and —N(R^(23i))S(O)₂R^(23j); R^(23a) to R^(23j) independently represent C₁₋₆ alkyl, aryl or R^(23a) to R^(23i) independently represent H; A represents a direct bond, —J—, —J—N(R²⁴)— or —J—O— (in which latter two groups, N(R²⁴)— or O— is attached to the carbon atom bearing R⁴ and R⁵); B represents —Z—, —Z—N(R²⁵)—, —N(R²⁵)—Z—, —Z—S(O)_(n)—, —Z—O— (in which latter two groups, Z is attached to the carbon atom bearing R⁴ and R⁵), —N(R²⁵)C(O)O—Z—, (in which latter group, —N(R²⁵) is attached to the carbon atom bearing R⁹ and R¹⁰) or —C(O)N(R²⁵)— (in which latter group, —C(O) is attached to the carbon atom bearing R⁴ and R⁵); J represents C₁₋₆ alkylene optionally substituted by one or more substituents selected from —OH, halo and amino; Z represents a direct bond or C₁₋₄ alkylene; R²⁴ and R²⁵ independently represent H or C₁₋₆ alkyl; G represents CH or N; R⁶ represents one or more optional substituents selected from —OH, cyano, halo, nitro, C₁₋₆ alkyl (optionally terminated by —N(H)C(O)OR^(26a)), C₁₋₆ alkoxy, —N(R^(27a))R^(27b), —C(O)R^(27c), —C(O)OR^(27d), —C(O)N(R^(27e))R^(27f), —N(R^(27g))C(O)R^(27h), —N(R^(27i))C(O)N(R^(27j))R^(27k), —N(R^(27m))S(O)₂R^(26b), —S(O)_(n)R^(26c), and/or —OS(O)₂R^(26d); R^(26a) to R^(26d) independently represent C₁₋₆ alkyl; R^(27a) to R^(27m) independently represent H or C₁₋₆ alkyl; n represents, at each occurrence, 0, 1 or 2; and R^(a) to R^(h) and R³ independently represent H or C₁₋₄ alkyl; wherein each aryl and aryloxy group, unless otherwise specified, is optionally substituted; or a pharmaceutically acceptable derivative thereof; provided that (a) when A represents —J—N(R²⁴)— or —J—O—, then: (i) J does not represent C₁ alkylene; and (ii) B does not represent —N(R²⁵)—, —N(R²⁵)—Z— (in which latter group N(R²⁵) is attached to the carbon atom bearing R⁴ and R⁵), —S(O)_(n)—, —O— or —N(R²⁵)C(O)O—Z— when R⁴ and R⁵ do not together represent ═O; (b) when R⁴ represents —OR¹⁸ or —N(R¹⁹)(R²⁰), then: (i) A does not represent —J—N(R²⁴)— or —J—O—; and (ii) B does not represent —N(R²⁵)—, —N(R²⁵)—Z— (in which latter group N(R²⁵) is attached to the carbon atom bearing R⁴ and R⁵), —S(O)_(n)—, —O— or —N(R²⁵)C(O)O—Z—; (c) when A represents a direct bond, then R⁴ and R⁵ do not together represent ═O; and (d) the compound is not: (±) (8β)-4-amino-5-chloro-2-methoxy-N-(3-benzyl-3-azabicyclo[3.2.1]oct-8-yl)benzamide; (S)-N-(3-benzyl-3-azabicyclo[3.2.1]oct-8-yl)-4-amino-5-chloro-2-(1-methyl-2-butynyl)oxybenzamide; or (S)-N-(3-benzyl-3-azabicyclo[3.2.1]oct-8-yl)-4-amino-5-chloro-2-(1-methyl-2-butynyl)oxybenzamide hydrochloride.
 2. A compound as claimed in claim 1, wherein the optional substituents on aryl and aryloxy groups are one or more groups selected from —OH, halo, Het¹, cyano, nitro, C₁₋₆ alkyl, C₁₋₆ alkoxy, —N(R^(27a))R^(27b), —C(O)R^(27c), —C(O)OR^(27d), —C(O)N(R^(27e))R^(27f), —N(R^(27g))C(O)R^(27h), —N(R^(27m))S(O)₂R^(26b), —S(O)_(n)R^(26c), and/or —OS(O)₂R^(26d), wherein Het¹, R^(26b) to R^(26d), R^(27a) to R^(27m) and n are as defined in claim 1, provided that when substituted by one or more Het¹ group(s), any aryl group(s) that said Het¹ group(s) may be substituted with may not itself (themselves) be substituted by any Het¹ group(s).
 3. A compound as claimed in claim 1, wherein R^(a) to R^(h) all represent H.
 4. A compound as claimed in claim 1, wherein R^(1a) represents C₁₋₈ alkyl (optionally substituted and/or terminated by one or more groups selected from halo, optionally substituted aryl, Het¹, —C(O)R^(7a), —OR^(7b), —N(R⁸)R^(7c), —C(O)XR⁹, —C(O)N(R¹⁰)R^(7d) and —S(O)₂R¹¹), Het², —C(O)R^(7a), —C(O)XR⁹, —C(O)N(R¹⁰)R^(7d) or —S(O)₂R¹¹.
 5. A compound as claimed in claim 4, wherein R^(7a) to R^(7d) independently represent, at each occurrence, H, C₁₋₅ alkyl (optionally substituted and/or terminated by one or more substituents selected from —OH, C₁₋₄ alkoxy, halo, cyano, optionally substituted aryl, Het³ and —NHC(O)R¹²), optionally substituted aryl or Het⁴, or R^(7d), together with R¹⁰, represents C₃₋₆ alkylene.
 6. A compound as claimed in claim 5, wherein R¹² represents C₁₋₃ alkyl (optionally substituted and/or terminated by one or more substituents selected from halo, aryl and —NHC(O)R¹³) or optionally substituted aryl.
 7. A compound as claimed in claim 6, wherein R¹³ represents C₁₋₃ alkyl or aryl.
 8. A compound as claimed in claim 1, wherein R⁸ represents H, C₁₋₄ alkyl (optionally substituted and/or terminated by optionally substituted aryl), optionally substituted aryl, —C(O)R^(14a) or —C(O)OR^(14b).
 9. A compound as claimed in claim 8, wherein R^(14a) and R^(14b) represent C₁₋₄ alkyl (optionally substituted and/or terminated by aryl) or aryl.
 10. A compound as claimed in 1, wherein R⁹ represents, at each occurrence, C₁₋₈ alkyl (optionally substituted and/or terminated by one or more substituents selected from —OH, halo, cyano, optionally substituted aryl, C₁₋₄ alkoxy, —SO₂R¹⁵ and Het⁵).
 11. A compound as claimed in claim 10, wherein R¹⁵ represents C₁₋₄ alkyl or aryl.
 12. A compound as claimed in 1, wherein R¹⁰ represents, at each occurrence, H, C₁₋₈ alkyl, C₁₋₄ alkoxy (which latter two groups are optionally substituted and/or terminated by one or more substituents selected from —OH, halo and C₁₋₄ alkoxy), —D-(optionally substituted aryl), —D-aryloxy, —D—Het⁶, —D—S(O)₂R^(17a), or R¹⁰, together with R^(7d), represents C₃₋₆ alkylene.
 13. A compound as claimed in claim 12, wherein R^(17a) represents C₁₋₄ alkyl or optionally substituted aryl.
 14. A compound as claimed in claim 1, wherein D represents a direct bond or C₁₋₃ alkylene.
 15. A compound as claimed in claim 1, wherein R¹¹ represents, at each occurrence, C₁₋₅ alkyl (optionally substituted and/or terminated by one or more halo atoms), optionally substituted aryl or Het⁷.
 16. A compound as claimed in claim 1, wherein R⁴ represents H, halo, C₁₋₂ alkyl, —OR¹⁸ or —E—N(R¹⁹)R²⁰.
 17. A compound as claimed in claim 1, wherein R⁵ represents H, or C₁₋₂ alkyl.
 18. A compound as claimed in claim 1, wherein R¹⁸ represents H, C₁₋₄ alkyl, —E-(optionally substituted aryl) or —E—Het⁸.
 19. A compound as claimed in claim 1, wherein R¹⁹ represents H, C₁₋₄ alkyl, —E-aryl, —E—Het⁸, —C(O)R^(21a) or —C(O)OR²¹b.
 20. A compound as claimed in claim 1, wherein R²⁰ represents H, C₁₋₄ alkyl or —E-aryl.
 21. A compound as claimed in claim 1, wherein R^(21a) and R^(21b) independently represent C₁₋₄ alkyl (optionally substituted and/or terminated by one or more substituents selected from halo and aryl) or aryl.
 22. A compound as claimed in claim 1, wherein E represents, at each occurrence, a direct bond or C₁₋₂ alkylene.
 23. A compound as claimed in claim 1, wherein Het¹ to Het⁸ (as appropriate) independently represent, at each occurrence, fully saturated, wholly aromatic, partly aromatic and/or bicyclic five- to twelve-membered heterocyclic groups containing between one and four heteroatoms selected from oxygen, nitrogen and/or sulfur, which groups are optionally substituted by one or more substituents selected from oxo, halo, cyano, C₁₋₅ alkyl, C₁₋₄ alkoxy, —N(R^(23a))R^(23b), —C(O)R^(23c), —C(O)OR^(23d), —C(O)N(R^(23e))R^(23f), and —N(R^(23g))C(O)R^(23h).
 24. A compound as claimed in claim 23, wherein R^(23a) to R^(23h) independently represent H or C₁₋₃ alkyl.
 25. A compound as claimed in claim 1, wherein A represents a direct bond or —J—.
 26. A compound as claimed in claim 1, wherein B represents —Z—, —Z—N(R²⁵)—, —Z—S(O)_(n)— or —Z—O— (in which latter three groups, Z is attached to the carbon atom bearing R⁴ and R⁵).
 27. A compound as claimed in claim 1, wherein J represents C₁₋₅ alkylene optionally substituted by one or more substituents selected from —OH, halo and amino.
 28. A compound as claimed in claim 1, wherein Z represents a direct bond or C₁₋₃ alkylene.
 29. A compound as claimed in claim 1, wherein n represents 0 or
 2. 30. A compound as claimed in claim 1, wherein R²⁵ represents H or C₁₋₄ alkyl.
 31. A compound as claimed in claim 1, wherein G represents CH.
 32. A compound as claimed in claim 1, wherein R⁶ represents one or more optional substituents selected from —OH, cyano, halo, nitro, C₁₋₃ alkyl (optionally terminated by —N(H)C(O)OR^(26a)) and C₁₋₄ alkoxy.
 33. A compound as claimed in claim 32, wherein R⁶ represents one or two cyano groups.
 34. A compound as claimed in claim 1, wherein R^(26a) represents C₁₋₄ alkyl.
 35. A compound as claimed in claim 1, wherein R³ represents H or C₁₋₂ alkyl.
 36. A pharmaceutical formulation including a compound as defined in claim 1 in admixture with a pharmaceutically-acceptable adjuvant, diluent or carrier.
 37. A method of prophylaxis or treatment of an arrhythmia which method comprises administration of a therapeutically effective amount of a compound as defined in claim 10 a person suffering from, or susceptible to, such a condition.
 38. A process for the preparation of a compound of formula I as defined in claim 1 which comprises: (a) reaction of a compound of formula IIA or IIB,

wherein R¹, R², R³ and R^(a) to R^(h) are as defined in claim 1, with a compound of formula III, R²⁸—L¹  III wherein R²⁸ represents (as appropriate) either R¹ or R², L¹ represents a leaving group and R¹ and R² are as defined in claim 1; (b) for compounds of formula I in which R¹ or R² (as appropriate) represents —C(O)XR⁹ or —C(O)N(R¹⁰)R^(7d), reaction of a compound of formula IVA or IVB,

wherein R³ and R^(a) to R^(h) are as defined in claim 1, L¹ is as defined above, and R¹ and R² represent a fragment of formula Ia, as defined in claim 1, with a compound of formula V, R³⁰—H  V wherein R³⁰ represents —XR⁹ or —N(R¹⁰)R^(7d) and R^(7d), R⁹, R¹⁰ and X are as defined in claim 1; (c) for compounds of formula I in which R¹ or R² (as appropriate) represents —C(O)N(H)R¹⁰, reaction of a compound of formula IIA or IIB (as appropriate), as defined above (except that R¹ or R² (as appropriate) does not represent R^(1a)), with a compound of formula VI, R¹⁰—N═C═O  VI wherein R¹⁰ is as defined in claim 1; (d) for compounds of formula I in which R¹ or R² (as appropriate) represents a fragment of formula Ia in which A represents CH₂ and R⁴ represents —OH or —N(H)R¹⁹, reaction of a compound of formula IIA or IIB, as defined above (except that R¹ or R² (as appropriate) does not represent a fragment of formula Ia), with a compound of formula VII,

wherein Y represents O or N(R¹⁹) and R⁵, R⁶, R¹⁹, B and G are as defined in claim 1; (e) for compounds of formula I in which, in the fragment of formula Ia, B represents —Z—O—, reaction of a compound of formula VIIIA or VIIIB,

wherein R³, R⁴, R⁵, R^(a) to R^(h), A and Z are as defined in claim 1, and R¹ and R² (as appropriate) are as defined in claim 1 (except that, in each case, they do not represent a fragment of formula Ia), with a compound of formula IX,

wherein R⁶ and G are as defined in claim 1; (f) for compounds of formula I in which G represents N and B represents —Z—O—, reaction of a compound of formula VIIIA or VIIIB, as defined above, with a compound of formula X,

wherein L² represents a leaving group and R⁶ is as defined in claim 1; (g) for compounds of formula I in which R⁴ represents —OR¹⁸, in which R¹⁸ represents C₁₋₆ alkyl, —E-aryl or —E—Het⁸, reaction of a corresponding compound of formula I in which R⁴ represents OH with a compound of formula XI, R^(18a)OH  XI wherein R^(18a) represents C₁₋₆ alkyl, —E-aryl or —E—Het⁸, and E and Het⁸ are as defined in claim 1; (h) for compounds of formula I in which R⁴ represents —OR¹⁸, in which R¹⁸ represents C₁₋₆ alkyl, —E-aryl or —E—Het⁸, reaction of a compound of formula XIIA or XIIB,

wherein R¹ or R² (as appropriate) represents R^(1a), and R^(1a), R³, R⁵, R⁶, R^(a) to R^(h), A, B, G are as defined in claim 1 and L² is as defined above, with a compound of formula XI, as defined above; (i) for compounds of formula I in which R⁴ represents —E—NH₂, reduction of a compound of formula XIIIA or XIIIB,

wherein R¹ or R² (as appropriate) represents R^(1a), and R^(1a), R³, R⁵, R⁶, R^(a) to R^(h), A, B, E and G are as defined in claim 1; (j) for compounds of formula I in which R⁴ represents —E—N(R¹⁹)R²⁰, wherein R¹⁹ represents C₁₋₆ alkyl, —E-aryl —E—Het⁸, —C(O)R^(21a), —C(O)OR^(21b), —S(O)₂R^(21c) or —C(O)N(R^(22a))R^(22b), reaction of a corresponding compound of formula I in which R⁴ represents —E—N(H)R²⁰ with a compound of formula XIV, R^(19a)—L¹  XIV wherein R^(19a) represents C₁₋₆ alkyl, —E-aryl —E—Het⁸, —C(O)R^(21a), —C(O)OR^(21b), —S(O)₂R^(21c) or —C(O)N(R^(22a))R^(22b), and R^(21a), R^(21b), R^(21c), R^(22a), R^(22b), Het⁸ and E are as defined in claim 1 and L¹ is as defined above; (k) for compounds of formula I in which R⁴ represents —E—N(R²⁰)C(O)N(H)R^(22a), reaction of a corresponding compound of formula I in which R⁴ represents —E—N(H)R²⁰ with a compound of formula XV, R^(22a)—N═C═O  XV wherein R^(22a) is as defined in claim 1; (l) for compounds of formula I in which R⁴ represents —E—N(H)[C(O)]₂NH₂, reaction of a corresponding compound of formula I in which R⁴ represents —E—NH₂ with oxalic acid diamide; (m) for compounds of formula I in which R⁴ represents —E—N(H)C(NH)NH₂, reaction of a corresponding compound of formula I in which R⁴ represents —E—NH₂ with a compound of formula XVI, R²⁹O—C(═NH)NH₂  XVI or an N-protected derivative thereof, wherein R²⁹ represents C₁₋₁₀ alkyl or aryl, which groups are optionally substituted by one or more halo or nitro groups; (n) for compounds of formula I in which R⁴ represents —OR¹⁸, in which R¹⁸ represents —C(O)R^(21a), —C(O)OR^(21b) or —C(O)N(R^(22a))R^(22b), reaction of a corresponding compound of formula I in which R⁴ represents —OH with a compound of formula XVII, R^(18b)—L³  XVII wherein R^(18b) represents —C(O)R^(21a), —C(O)OR^(21b) or —C(O)N(R^(22a))R^(22b), L³ represents a leaving group and R^(21a), R^(21b), R^(22a) and R^(22b) are as defined in claim 1; (o) for compounds of formula I in which R⁴ represents H or —OH and R⁵ represents H, reduction of a corresponding compound of formula I in which R⁴ and R⁵ together represent ═O; (p) for compounds of formula I in which R⁴ represents halo, substitution of a corresponding compound of formula I in which R⁴ represents —OH, using a halogenating agent; (q) for compounds of formula I in which R⁴ and R⁵ represent H, A represents —J— and B represents —N(R²⁵)—Z— (wherein —N(R²⁵) is attached to the carbon atom bearing R⁴ and R⁵), reaction of a compound of formula XVIIIA or XVIIIB,

wherein R¹ or R² (as appropriate) represents R^(1a), and R^(1a), R³, R⁴, R⁵, R²⁵, R^(a) to R^(h) and J are as defined in claim 1, with a compound of formula XIX,

wherein R⁶, G and Z are as defined in claim 1 and L² is as defined above; (r) for compounds of formula I in which A represents C₂ alkylene and R⁴ and R⁵ together represent ═O, reaction of a compound of formula IIA or IIB, as defined above (except that R¹ or R² (as appropriate) does not represent a fragment of formula Ia), with a compound of formula XX,

wherein B, G and R⁶ are as defined in claim 1; (s) for compounds of formula I in which R³ represents H and R² represents unsubstituted C₁₋₄ alkyl, reaction of a compound of formula XXI,

wherein R⁴, R⁵, R⁶, R^(a) to R^(h), A, B and G are as defined in claim 1, with a compound of formula XXII, R³¹—NH₂  XXII wherein R³¹ represents unsubstituted C₁₋₄ alkyl, in the presence of a reducing agent; (t) for compounds of formula I in which R¹ represents —C(O)OR⁹ and R^(a) and/or R^(b) represent C₁₋₄ alkyl, reaction of a corresponding compound of formula I in which R¹ represents —C(O)OR⁹ and R^(a) and R^(b) represent H with one or more equivalents of a compound of formula XXIII, R³²—L⁴  XXIII wherein R³² represents C₁₋₄ alkyl and L⁴ is a leaving group, in the presence of a strong base; (u) for compounds of formula I which are 3-azabicyclo[3.2.1]octane-nitrogen N-oxide derivatives, oxidation of the corresponding 3-azabicyclo-[3.2.1]octane nitrogen of a corresponding compound of formula I, in the presence of an oxidising agent; (v) for compounds of formula I which are C₁₋₄ alkyl quaternary ammonium salt derivatives, in which the alkyl group is attached to a 3-azabicyclo[3.2.1]octane nitrogen, reaction, at the 3-azabicyclo[3.2.1]octane nitrogen, of a corresponding compound of formula I with a compound of formula XXIII, as defined above; (w) conversion of one R⁶ substituent to another; or (x) deprotection of a protected derivative of a compound of formula I as defined in claim
 1. 39. A compound of formula IIA or IIB, as defined in claim 38, or a protected derivative thereof, provided that the compound is not: (±) (8α,β)-3-ethyl-3-azabicyclo[3.2.1]octan-8-amine; 8-amino-3-methyl-3-azabicyclo[3.2.1]octane; 8-amino-3-isopropyl-3-azabicyclo[3.2.1]octane; 8-amino-3-benzyl-3-azabicyclo[3.2.1]octane; 3-{2-[4-(6-aminopyridin-2-yl)phenyl]ethyl}-3-azabicyclo[3.2.1]oct-8-ylamine; or 3-azabicyclo[3.2.1]oct-8-ylamine t-butylcarbamate.
 40. A compound of formula IVA or IVB, as defined in claim 38, or a protected derivative thereof.
 41. A compound of formula VIIIA or VIIIB, as defined in claim 38, or a protected derivative thereof.
 42. A compound of formula XIIA or XIIB, as defined in claim 38, or a protected derivative thereof.
 43. A compound of formula XIIIA or XIIIB, as defined in claim 38, or a protected derivative thereof.
 44. A compound of formula XVIIIA or XVIIIB, as defined in claim 38, or a protected derivative thereof.
 45. A compound of formula XXI, as defined in claim 38 (provided that when R^(a) to R^(h) all represent H, G represents CH and R⁶ is absent, then the group —A—C(R⁴)(R⁵)—B— does not represent unsubstituted ethyl), or a protected derivative thereof.
 46. A compound of formula XXIV,

wherein R³ and R^(a) to R^(h) are as defined in claim 1 (provided that R^(a) to R^(h) do not all represent H), or a protected derivative thereof.
 47. A method as claimed in claim 37 wherein the arrhythmia is an atrial or a ventricular arrhythmia. 